clinic

Snoqualmie Valley Hospital

5 Stars (24 Reviews)

Snoqualmie Valley Hospital is a clinic that specializes in DPC Family Medicine and Concierge Pediatrics. The clinic is located in Snoqualmie, Washington. Snoqualmie Valley Hospital is known for housing expert physicians. Snoqualmie Valley Hospital offers all the services, treatments and procedures pertinent to the specialties mentioned above.

4 Doctors | Website
About Snoqualmie Valley Hospital

"Welcome to Snoqualmie Valley Hospital Dedicated to quality. Devoted to community. The Snoqualmie Valley Hospital staff is dedicated to providing expert, compassionate, quality care to the communities of Carnation, Fall City, North Bend, Preston, Snoqualmie, Snoqualmie Pass, and surrounding areas. The board-certified and specially-trained staff provides uncompromising quality of care. The modern Hospital is designated by the Washington State Department of Health as a Trauma Level 5 hospital. Additionally the Hospital has from the Department of Health categorization as a Cardiac Level 2 and Stroke Level 3 facility. Services include a Emergency and Trauma Care, Primary Care, Inpatient and Outpatient Rehabilitation, Lab Services, Diagnostic Imaging and Endoscopy/Colonoscopy procedures. Specialty services include cardiology, gastroenterology, sports medicine and physical rehabilitation, mental health, and pediatric care."

Address

35020 Southeast Kinsey Street Snoqualmie,
WA 98065

Modes of Payment

Card | Cash


Providers
Filters
Ron Spiegel - 35020 Southeast Kinsey Street, Snoqualmie, Washington, 98065
Snoqualmie Valley Hospital
Concierge Pediatrics
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
35020 Southeast Kinsey Street, Snoqualmie, WA 98065
Alan Johnson - 35020 Southeast Kinsey Street, Snoqualmie, Washington, 98065
Snoqualmie Valley Hospital
DPC Family Medicine
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
35020 Southeast Kinsey Street, Snoqualmie, WA 98065
Joanna Hagen - 35020 Southeast Kinsey Street, Snoqualmie, Washington, 98065
Snoqualmie Valley Hospital
DPC Family Medicine
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
35020 Southeast Kinsey Street, Snoqualmie, WA 98065
John Gray - 35020 Southeast Kinsey Street, Snoqualmie, Washington, 98065
Snoqualmie Valley Hospital
DPC Family Medicine
Fee $0 - $0
Max no. of Patients: N/A
Accepting New Patients: NA
35020 Southeast Kinsey Street, Snoqualmie, WA 98065

Reviews
Posted by FMDD User
May 11, 2022
Dr. Gray is the best physician I've ever met! He isn't afraid to spend his time with his patients, even if it means running late. He always speaks to you frankly but gently. He's simply the BESTT

Review For John Gray

Posted by FMDD User
January 31, 2022
He listens and he remembers the small stuff.

Review For John Gray

Posted by FMDD User
April 14, 2022
I recently moved and am hoping to find a doctor who is even a tenth as compassionate and intuitive as Dr. Gray. Thank you for your years of support DOC and we hope to see you again soon.

Review For John Gray

Posted by FMDD User
May 03, 2022
Wish I could give him ten stars. He is the best of the best.

Review For John Gray


Conditions Treated
  • Torticollis
  • Lactose intolerance
  • Kidney infection
  • Stroke
  • Kawasaki disease
  • Irritable bowel syndrome
  • Melanoma
  • Insomnia
  • Inguinal hernia
  • Swimmer's ear
  • Meningitis
  • Hydrocele
  • Hiatal hernia
  • Milia
  • Testicular torsion
  • Molluscum contagiosum
  • Hemangioma
  • Scleroderma
  • Multiple sclerosis
  • Harlequin ichthyosis
  • Scurvy
  • Narcolepsy
  • Nausea
  • Generalized anxiety disorder
  • Gallstones
  • Fifth disease
  • Tinea versicolor
  • Eczema
  • Osteomyelitis
  • Sepsis
  • Smallpox
  • Tourette syndrome
  • Diphtheria
  • Diabetes
  • Dermatitis
  • Depression
  • Deep vein thrombosis
  • Seizures
  • Cystic fibrosis
  • Congestive heart failure
  • Concussion
  • Chronic fatigue syndrome
  • Ulcerative colitis
  • Cellulitis
  • Celiac disease
  • Umbilical hernia
  • Pityriasis rosea
  • Strep throat
  • Hand-foot-and-mouth disease
  • Ear infection
  • Croup
  • Cerebral palsy
  • Cardiomyopathy
  • Canker sore
  • Psoriasis
  • Back pain
  • Skin cancer
  • Pulmonary embolism
  • Atopic dermatitis
  • Asperger's syndrome
  • Rectal prolapse
  • Restless legs syndrome
  • Vitiligo
  • Rosacea
  • Roseola
  • Sarcoidosis
  • Sjogren's syndrome
  • Scarlet fever
  • Liver disease
  • Strabismus
  • Lupus
  • Autism spectrum disorder
  • Asthma
  • Adhd
  • Upper respiratory infection
  • Muscle strains
  • Hemorrhoids
  • Hyperthyroidism
  • Eating disorders
  • Menopause
  • Hypertension
  • Tennis elbow
  • Rotator cuff
  • Covid-19 testing
  • Tension headache
  • Arrhythmias
  • Anal fissure
  • Gout
  • Hypothyroidism
  • Allergies
  • High cholesterol
  • Sleep apnea
  • High blood pressure
  • Acid reflux
  • Measles
  • Pneumonia
  • Cervical cancer
  • Acute pharyngitis
  • Allergic conjunctivitis
  • Allergic cough
  • Allergic rhinitis
  • Anhidrosis
  • Aniridia
  • Bad breath
  • Beriberi
  • Black hairy tongue
  • Burning mouth syndrome
  • Candidiasis
  • Carbuncle
  • Castleman disease
  • Cat scratch disease
  • Central sleep apnea
  • Cherry angioma
  • Chikungunya
  • Cholera
  • Cholesteatoma
  • Chronic bronchitis
  • Chronic cough
  • Chronic headache
  • Chronic illness
  • Chronic obstructive pulmonary disease
  • Chronic sinusitis
  • Cold urticaria
  • Comedones
  • Coronary artery disease
  • Coronary heart disease
  • Crooked teeth
  • Cyclic vomiting syndrome
  • De quervain's
  • Delayed ejaculation
  • Dengue fever
  • Dermatitis herpetiformis
  • Dextrocardia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diaphragmatic hernia
  • Dilated cardiomyopathy
  • Diphallia
  • Dry eye
  • Dry mouth
  • Ehrlichiosis
  • Enlarged prostate
  • Episcleritis
  • Essential tremor
  • Exocrine pancreatic insufficiency
  • Farsightedness
  • Fecal impaction
  • Femoral hernia
  • Gastroesophageal reflux disease (gerd)
  • Gigantism
  • Gilbert syndrome
  • Glomerulonephritis
  • Glossitis
  • Granuloma annulare
  • Granulomatosis with polyangiitis
  • Grover's disease
  • Gum disease
  • Guttate psoriasis
  • Hashimoto thyroiditis
  • Hearing loss
  • Heart block
  • Heart disease
  • Hemolysis
  • Hemolytic anemia
  • Herpangina
  • Hiv aids
  • Hyperopia
  • Hyperparathyroidism
  • Hypoparathyroidism
  • Iga nephropathy
  • Inflammatory bowel disease
  • Influenza
  • Interstitial cystitis
  • Intertrigo
  • Iron deficiency anemia
  • Ischemic heart disease
  • Keratitis
  • Keratoconus
  • Kidney disease
  • Legionnaire disease
  • Leishmaniasis
  • Lemierre syndrome
  • Leptospirosis
  • Leukocytosis
  • Lichen sclerosis
  • Lichen simplex chronicus
  • Liver spots
  • Long qt syndrome
  • Loose teeth
  • Low blood sugar
  • Low sodium level
  • Lungs
  • Lymphocytic colitis
  • Lymphogranuloma venereum
  • Magnesium deficiency
  • Malabsorption
  • Male pattern baldness
  • Malignant hyperthermia
  • May thurner syndrome
  • Melioidosis
  • Men's health
  • Meth addiction
  • Methemoglobinemia
  • Mitral regurgitation
  • Mitral valve prolapse
  • Mitral valve regurgitation
  • Mittelschmerz
  • Mixed connective tissue disease
  • Morning sickness
  • Mouth sores
  • Paroxysmal supraventricular tachycardia
  • Pellagra
  • Peptic ulcer
  • Peptic ulcer disease
  • Polymyalgia rheumatica
  • Primary care
  • Protein deficiency
  • Pulmonary fibrosis
  • Reye syndrome
  • Septicemia
  • Serum sickness
  • Situs inversus
  • Superficial thrombophlebitis
  • Thrombophlebitis
  • Trimethylaminuria
  • Vasoconstriction
  • Vitamin b12 deficiency
  • Anencephaly
  • Apert syndrome
  • Aphantasia
  • Apraxia
  • Beckwith wiedemann syndrome
  • Birthmarks
  • Blount disease
  • Brachydactyly
  • Cafe au lait spots
  • Caput succedaneum
  • Caudal regression syndrome
  • Cerebellar hypoplasia
  • Choanal atresia
  • Clubfoot
  • Congenital adrenal hyperplasia
  • Congenital diaphragmatic hernia
  • Congenital heart disease
  • Cornelia de lange syndrome
  • Craniosynostosis
  • Cri du chat syndrome
  • Crouzon syndrome
  • Cystic hygroma
  • Cystinosis
  • Dandy walker syndrome
  • Digeorge syndrome
  • Dravet syndrome
  • Duchenne muscular dystrophy
  • Ebstein's anomaly
  • Ectodermal dysplasias
  • Encephalocele
  • Encopresis
  • Epicanthal folds
  • Epispadias
  • Erb's palsy
  • Esophageal atresia
  • Esotropia
  • Ewing sarcoma
  • Exercise induced asthma
  • Fanconi anemia
  • Food allergy
  • Fragile x syndrome
  • Galactosemia
  • Gastroschisis
  • Gingivostomatitis
  • Growth hormone deficiency
  • Head lice
  • Hemolytic uremic syndrome
  • Hemophilia a
  • Henoch schonlein purpura
  • Hermansky pudlak syndrome
  • Hirschsprung disease
  • Holoprosencephaly
  • Horseshoe kidney
  • Hydranencephaly
  • Hydrops fetalis
  • Hypophosphatasia
  • Hypoplastic left heart syndrome
  • Hypospadias
  • Hypotonia
  • Intussusception
  • Juvenile dermatomyositis
  • Juvenile idiopathic arthritis
  • Kabuki syndrome
  • Knock knees
  • Krabbe disease
  • Kwashiorkor
  • Langerhans cell histiocytosis
  • Laryngomalacia
  • Lazy eye
  • Legg calve perthes disease
  • Lennox gastaut syndrome
  • Lesch nyhan syndrome
  • Lissencephaly
  • Maple syrup urine disease
  • Microcephaly
  • Micrognathia
  • Microtia
  • Moebius syndrome
  • Mumps
  • Munchausen syndrome by proxy
  • Myelomeningocele
  • Necrotizing enterocolitis
  • Neonatal abstinence syndrome
  • Nephrotic syndrome
  • Neuroblastoma
  • Newborn jaundice
  • Noma
  • Noonan syndrome
  • Omphalocele
  • Osgood schlatter disease
  • Osteogenesis imperfecta
  • Otitis
  • Otitis media
  • Parainfluenza
  • Patent ductus arteriosus
  • Pectus carinatum
  • Pectus excavatum
  • Pertussis
  • Pfeiffer syndrome
  • Phenylketonuria
  • Pityriasis alba
  • Plagiocephaly
  • Poland syndrome
  • Polydactyly
  • Pompe disease
  • Precocious puberty
  • Progeria
  • Purpura
  • Rett syndrome
  • Rhabdomyosarcoma
  • Rheumatic fever
  • Rickets
  • Rubella
  • Selective mutism
  • Sotos syndrome
  • Spinal muscular atrophy
  • Stickler syndrome
  • Stork bite
  • Sturge weber syndrome
  • Sudden infant death syndrome
  • Syndactyly
  • Tay sachs disease
  • Temper tantrums
  • Tetralogy of fallot
  • Thalassemia
  • Treacher collins syndrome
  • Truncus arteriosus
  • Tuberous sclerosis
  • Uncombable hair syndrome
  • Undescended testicle
  • Ventricular septal defects
  • Wilms tumor
  • Aarskog syndrome
  • Abo incompatibility
  • Acrodermatitis enteropathica
  • Acute flaccid myelitis
  • Acute otitis externa
  • Adams oliver syndrome
  • Add adhd
  • Adenosine deaminase deficiency
  • Adrenoleukodystrophy
  • Aicardi goutieres syndrome
  • Aicardi syndrome
  • Albright's hereditary osteodystrophy
  • Alexander disease
  • Cramps
  • Sore throat
  • Alopecia totalis
  • Alopecia universalis
  • Alstrom syndrome
  • Alternating hemiplegia of childhood
  • Amebiasis
  • Anaplastic large cell lymphoma
  • Anaplastic thyroid cancer
  • Angiodysplasia of the colon
  • Angioimmunoblastic t cell lymphoma
  • Anisakiasis
  • Annular pancreas
  • Annular tears
  • Anorectal abscess
  • Anti nmda receptor encephalitis
  • Antisynthetase syndrome
  • Anton syndrome
  • Aortic regurgitation
  • Aortic valve stenosis
  • Aphthous stomatitis
  • Aplasia cutis congenita
  • Apnea of prematurity
  • Appendix cancer
  • Aquablation
  • Arachnodactyly
  • Arrhythmogenic right ventricular cardiomyopathy
  • Arterial embolism
  • Arterial insufficiency
  • Arthrogryposis multiplex congenita
  • Asymptomatic bacteriuria
  • Ataxia telangiectasia
  • Athetosis
  • Atrial myxoma
  • Atrioventricular septal defect
  • Atypical pneumonia
  • Atypical teratoid rhabdoid tumor
  • Auditory neuropathy spectrum disorder
  • Autosomal dominant polycystic kidney disease
  • Avian influenza
  • Axenfeld rieger syndrome
  • Axial spondyloarthritis
  • Bacterial food poisoning
  • Bacterial gastroenteritis
  • Barber say syndrome
  • Bardet biedl syndrome
  • Barth syndrome
  • Bartter syndrome
  • Becker muscular dystrophy
  • Becker's nevus
  • Benign essential blepharospasm
  • Benign prostatic hypertrophy
  • Benign rolandic epilepsy
  • Bernard soulier syndrome
  • Biceps tendon rupture
  • Bilateral hydronephrosis
  • Bilateral perisylvian polymicrogyria
  • Bile acid malabsorption
  • Bile duct obstruction
  • Binder's syndrome
  • Biotinidase deficiency
  • Birdshot chorioretinopathy
  • Birt hogg dube syndrome
  • Bladder outlet obstruction
  • Blau syndrome
  • Blepharophimosis
  • Blind loop syndrome
  • Bloom syndrome
  • Blue rubber bleb nevus syndrome
  • Bowel incontinence
  • Bowenoid papulosis
  • Brachial plexopathy
  • Brain abscess
  • Brain herniation
  • Branchiootorenal syndrome
  • Breast cancer in men
  • Breast infection
  • Bronchial asthma
  • Bronchiolitis obliterans
  • Bronchogenic cyst
  • Bronchopulmonary dysplasia
  • Brown syndrome
  • Bulging fontanelles
  • Bursitis of the heel
  • Byssinosis
  • Calcinosis
  • Campomelic dysplasia
  • Campylobacter infection
  • Canavan disease
  • Cancer pain
  • Candida infection of the skin
  • Capsule endoscopy
  • Cardiac amyloidosis
  • Carditis
  • Carney complex
  • Caroli disease
  • Carotid artery disease
  • Carotid stenosis
  • Carpenter syndrome
  • Cartilage hair hypoplasia
  • Cat eye syndrome
  • Cavernous sinus thrombosis
  • Central pain syndrome
  • Central serous chorioretinopathy
  • Cerebellar degeneration
  • Cerebral amyloid angiopathy
  • Cerebral cavernous malformation
  • Cerebral hypoxia
  • Cervical disc herniations
  • Cervical spinal stenosis
  • Cervical spine disorders
  • Char syndrome
  • Chediak higashi syndrome
  • Cheilitis glandularis
  • Chemical pneumonitis
  • Cherubism
  • Chiari malformation type 2
  • Childhood disintegrative disorder
  • Chinese restaurant syndrome
  • Chondroblastoma
  • Chondrodysplasia
  • Chondroma
  • Chordoma
  • Choriocarcinoma
  • Choroid plexus cyst
  • Choroid plexus papilloma
  • Choroideremia
  • Chromoblastomycosis
  • Chromophobe renal cell carcinoma
  • Chronic granulomatous disease
  • Chronic idiopathic constipation
  • Chronic inflammatory demyelinating polyneuropathy
  • Chronic myelogenous leukemia
  • Chronic myelomonocytic leukemia
  • Chronic renal disease
  • Chronic subdural hematoma
  • Chylous ascites
  • Cicatricial pemphigoid
  • Claw foot
  • Clear cell sarcoma
  • Cleft lip and palate
  • Cleft palate and cleft lip
  • Cloacal exstrophy
  • Cloudy cornea
  • Cmv retinitis
  • Coats disease
  • Cockayne syndrome
  • Coffin lowry syndrome
  • Coffin siris syndrome
  • Cogan's syndrome
  • Cohen syndrome
  • Cold and flu
  • Cold flu
  • Collagenous colitis
  • Coloboma of iris
  • Coloboma of optic nerve
  • Colorado tick fever
  • Cone rod dystrophy
  • Congenital cataract
  • Congenital generalized lipodystrophy
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Congenital lobar emphysema
  • Congenital myasthenic syndrome
  • Congenital syphilis
  • Congenital toxoplasmosis
  • Constrictive pericarditis
  • Cor triatriatum
  • Corns and calluses
  • Coronary artery spasm
  • Corpus callosum agenesis
  • Cortical dysplasia
  • Corticobasal degeneration
  • Costello syndrome
  • Cowden syndrome
  • Cramp fasciculation syndrome
  • Craniodiaphyseal dysplasia
  • Craniopharyngioma
  • Craniotabes
  • Creeping eruption
  • Crigler najjar syndrome
  • Crowded teeth
  • Cryptococcal meningitis
  • Cutaneous lupus erythematosus
  • Cutaneous t cell lymphoma
  • Cutis laxa
  • Medication management
  • Meds
  • Cutis marmorata telangiectatica congenita
  • Cyclic neutropenia
  • Cytomegalovirus infection
  • Donnai barrow syndrome
  • Duodenal atresia
  • Dystrophic epidermolysis bullosa
  • Ear tag
  • Eec syndrome
  • Eisenmenger syndrome
  • Ellis van creveld syndrome
  • Emery dreifuss muscular dystrophy
  • Endocardial cushion defect
  • Enlarged adenoids
  • Epidermolysis bullosa simplex
  • Evans syndrome
  • Exstrophy of the bladder
  • Fanconi syndrome
  • Fetal hydantoin syndrome
  • Floating harbor syndrome
  • Foxg1 syndrome
  • Fraser syndrome
  • Freeman sheldon syndrome
  • Frontonasal dysplasia
  • Fumarase deficiency
  • Ganglioneuroma
  • Gianotti crosti syndrome
  • Giant congenital melanocytic nevus
  • Glucose 6 phosphate dehydrogenase deficiency
  • Glutaric acidemia type 1
  • Gm1 gangliosidosis
  • Grass allergy
  • Hallermann streiff syndrome
  • Hemihyperplasia
  • Hemimegalencephaly
  • Hemolytic disease of the newborn
  • Hemophagocytic lymphohistiocytosis
  • Hemophilia b
  • Hepatoblastoma
  • Hereditary spherocytosis
  • Heterotaxy syndrome
  • Holt oram syndrome
  • Hypochondroplasia
  • Hypohidrotic ectodermal dysplasia
  • Hypomelanosis of ito
  • Imperforate anus
  • Incontinentia pigmenti
  • Infant botulism
  • Infantile pyloric stenosis
  • Infectious mononucleosis
  • Interrupted aortic arch
  • Jacobsen syndrome
  • Juvenile myoclonic epilepsy
  • Kohler disease
  • Koolen de vries syndrome
  • Landau kleffner syndrome
  • Laryngeal cleft
  • Linear nevus sebaceous syndrome
  • Lowe syndrome
  • Meatal stenosis
  • Meconium aspiration syndrome
  • Meningocele
  • Meningococcemia
  • Menkes disease
  • Menkes syndrome
  • Metopic ridge
  • Miller dieker syndrome
  • Miller syndrome
  • Mongolian blue spots
  • Muenke syndrome
  • Myoclonic epilepsy
  • Myotonia congenita
  • Nail patella syndrome
  • Nasal flaring
  • Nemaline myopathy
  • Neonatal conjunctivitis
  • Neonatal herpes
  • Neonatal sepsis
  • Nephrogenic diabetes insipidus
  • Nephronophthisis
  • Netherton syndrome
  • Neuronal ceroid lipofuscinoses
  • Newborn low blood sugar
  • Newborn transient tachypnea
  • Niemann pick disease
  • Otitis media with effusion
  • Periventricular leukomalacia
  • Pfapa
  • Pierre robin sequence
  • Pitt hopkins syndrome
  • Pituitary dwarfism
  • Polymicrogyria
  • Pontocerebellar hypoplasia
  • Porencephaly
  • Potocki lupski syndrome
  • Potter syndrome
  • Propionic acidemia
  • Prune belly syndrome
  • Pulmonary atresia
  • Pulmonary valve stenosis
  • Rasmussen encephalitis
  • Retinopathy of prematurity
  • Rhabdoid tumor
  • Rhabdomyosarcoma embryonal
  • Roberts syndrome
  • Robinow syndrome
  • Rubinstein taybi syndrome
  • Saethre chotzen syndrome
  • Scalded skin syndrome
  • Seckel syndrome
  • Severe combined immunodeficiency
  • Short stature
  • Single palmar crease
  • Sirenomelia
  • Slipped capital femoral epiphysis
  • Small for gestational age
  • Smith lemli opitz syndrome
  • Smith magenis syndrome
  • Spinal muscular atrophy type 1
  • Spondyloepiphyseal dysplasia
  • Sprengel deformity
  • Stereotypic movement disorder
  • Sunken fontanelles
  • Supravalvular aortic stenosis
  • Tetrasomy x
  • Thanatophoric dysplasia
  • Torch syndrome
  • Total anomalous pulmonary venous return
  • Toxic synovitis
  • Toxocariasis
  • Tracheobronchomalacia
  • Tracheoesophageal fistula
  • Transient tic disorder
  • Transposition of the great arteries
  • Tricuspid atresia
  • Triple x syndrome
  • Trisomy 14 mosaicism
  • Twin to twin transfusion syndrome
  • Vacterl association
  • Velopharyngeal insufficiency
  • Von gierke disease
  • Wagr syndrome
  • Weaver syndrome
  • West syndrome
  • Wiedemann steiner syndrome
  • Zellweger syndrome
  • Acalvaria
  • Achondrogenesis
  • Acrodysostosis
  • Acute bronchiolitis
  • Acute cerebellar ataxia
  • Adenylosuccinate lyase deficiency
  • Aec syndrome
  • Allan herndon dudley syndrome
  • Alpers huttenlocher syndrome
  • Alpha mannosidosis
  • Andersen disease
  • Aortopulmonary window
  • Arginase deficiency
  • Argininosuccinic aciduria
  • Arterial tortuosity syndrome
  • Aspartylglucosaminuria
  • Asphyxiating thoracic dystrophy
  • Aural polyps
  • Baller gerold syndrome
  • Bannayan riley ruvalcaba syndrome
  • Bartsocas papas syndrome
  • Behr syndrome
  • Beta ketothiolase deficiency
  • Bilirubin encephalopathy
  • Childhood pancreatitis
  • Chromosome 22 duplication
  • Chromosome 8p deletion
  • Classic galactosemia
  • Colonic atresia
  • Congenital anomalies of the heart
  • Congenital central hypoventilation syndrome
  • Congenital cytomegalovirus
  • Congenital heart block
  • Congenital hepatic fibrosis
  • Congenital mesoblastic nephroma
  • Congenital mirror movement disorder
  • Congenital nephrotic syndrome
  • Congenital radioulnar synostosis
  • Congenital sucrase isomaltase deficiency
  • Congenital tracheomalacia
  • Cytomegalic inclusion disease
  • Delayed growth
  • Diencephalic syndrome
  • Door syndrome
  • Dopa responsive dystonia
  • Double outlet left ventricle
  • Dubowitz syndrome
  • Duplication of urethra
  • Early infantile epileptic encephalopathy
  • Embryonal tumor with multilayered rosettes
  • Endocardial fibroelastosis
  • Fanconi bickel syndrome
  • Feingold syndrome
  • Femoral facial syndrome
  • Fetal cystic hygroma
  • Fg syndrome
  • Fryns syndrome
  • Fucosidosis
  • Gaba transaminase deficiency
  • Galactokinase deficiency
  • Galactosialidosis
  • Galloway mowat syndrome
  • Ganglioneuroblastoma
  • Gangliosidosis
  • Gastroesophageal reflux in infants
  • Gaucher disease type 2
  • Gaucher disease type 3
  • Geleophysic dysplasia
  • Giant congenital nevus
  • Glutaric acidemia type 2
  • H influenzae meningitis
  • Hennekam syndrome
  • Holocarboxylase synthetase deficiency
  • Icf syndrome
  • Idiopathic neutropenia
  • Idiopathic pulmonary hemosiderosis
  • Infant hearing loss
  • Infantile apnea
  • Infantile digital fibromatosis
  • Infantile myofibromatosis
  • Intestinal pseudo obstruction
  • Intraventricular hemorrhage of the newborn
  • Isovaleric acidemia
  • Jackson weiss syndrome
  • Johanson blizzard syndrome
  • Junctional epidermolysis bullosa
  • Juvenile myelomonocytic leukemia
  • Juvenile temporal arteritis
  • Kaufman oculocerebrofacial syndrome
  • Kerion celsi
  • Kindler syndrome
  • Kniest dysplasia
  • Knobloch syndrome
  • L1 syndrome
  • Lactate dehydrogenase deficiency
  • Lambdoid synostosis
  • Langer mesomelic dysplasia
  • Leri weill dyschondrosteosis
  • Lung agenesis
  • Mandibuloacral dysplasia
  • Marcus gunn phenomenon
  • Marden walker syndrome
  • Marinesco sjogren syndrome
  • Marshall smith syndrome
  • Marshall syndrome
  • Mass phenotype
  • Mckusick kaufman syndrome
  • Meckel syndrome
  • Medium chain acyl coa dehydrogenase deficiency
  • Megalencephaly capillary malformation syndrome
  • Meier gorlin syndrome
  • Mitral atresia
  • Mosaic trisomy 7
  • Mosaic trisomy 8
  • Mosaic trisomy 9
  • Mucolipidosis type 4
  • Mucopolysaccharidosis type 1
  • Mucopolysaccharidosis type 2
  • Mucopolysaccharidosis type 3
  • Myhre syndrome
  • Neonatal hemochromatosis
  • Neonatal hypothyroidism
  • Neonatal onset multisystem inflammatory disease
  • Newborn head molding
  • Newborn polycythemia
  • Nicolaides baraitser syndrome
  • Nijmegen breakage syndrome
  • Ohdo syndrome
  • Opitz g bbb syndrome
  • Opsoclonus myoclonus syndrome
  • Pallister hall syndrome
  • Pallister killian mosaic syndrome
  • Paroxysmal cold hemoglobinuria
  • Pediatric brain tumors
  • Pediatric myocarditis
  • Pediatric obesity
  • Peer relationships
  • Peho syndrome
  • Penoscrotal transposition
  • Pentasomy x
  • Perianal streptococcal cellulitis
  • Periventricular heterotopia
  • Perlman syndrome
  • Peters plus syndrome
  • Pik3ca related overgrowth spectrum
  • Pili torti
  • Pilonidal sinus disease
  • Pinealectomy
  • Pityriasis lichenoides et varioliformis acuta
  • Platelet storage pool deficiency
  • Pleuropulmonary blastoma
  • Popliteal pterygium syndrome
  • Post traumatic epilepsy
  • Prekallikrein deficiency
  • Premature infant
  • Primary amebic meningoencephalitis
  • Primary carnitine deficiency
  • Primitive neuroectodermal tumor
  • Progressive myoclonic epilepsy
  • Puberty disorder
  • Pulmonary atresia with intact ventricular septum
  • Pyridoxine deficiency
  • Pyruvate carboxylase deficiency
  • Rapadilino syndrome
  • Renpenning syndrome
  • Right ventricle hypoplasia
  • Ring chromosome 18
  • Rothmund thomson syndrome
  • Russell silver dwarfism
  • Satoyoshi syndrome
  • Scalp ear nipple syndrome
  • Schimke immuno osseous dysplasia
  • Schindler disease
  • Schinzel giedion syndrome
  • Schwartz jampel syndrome
  • Sea blue histiocytosis
  • Secondary immunodeficiency
  • Severe congenital neutropenia
  • Short chain acyl coa dehydrogenase deficiency
  • Short philtrum
  • Short qt syndrome
  • Short syndrome
  • Sialidosis
  • Simpson golabi behmel syndrome
  • Sjogren larsson syndrome
  • Smith kingsmore syndrome
  • Snyder robinson syndrome
  • Spinal muscular atrophy type 2
  • Spinal muscular atrophy type 3
  • Spondylocostal dysostosis
  • Spondyloepiphyseal dysplasia congenita
  • Sternal cleft
  • Stuve wiedemann syndrome
  • Subvalvular aortic stenosis
  • Temple syndrome
  • Tetra amelia syndrome
  • Tetrasomy 9p
  • Thrombocytopenia absent radius syndrome
  • Townes brocks syndrome
  • Tracheal agenesis
  • Transient erythroblastopenia of childhood
  • Trisomy 2 mosaicism
  • Van maldergem syndrome
  • Vici syndrome
  • Visceral larva migrans
  • Visceromegaly
  • Wiedemann rautenstrauch syndrome
  • And breastfeeding
  • Anomalous left coronary artery from the pulmonary artery
  • Anophthalmia plus syndrome
  • Arrhinia
  • Arterial calcification of infancy
  • Asphyxia neonatorum
  • Atresia of small intestine
  • Ballinger wallace syndrome
  • Beare stevenson cutis gyrata syndrome
  • Benign familial neonatal seizures
  • Berdon syndrome
  • Beta mannosidosis
  • Bowen conradi syndrome
  • C syndrome
  • Carey fineman ziter syndrome
  • Charlie m syndrome
  • Childhood acute myeloid leukemia
  • Childhood hypophosphatasia
  • Childhood iron deficiency anemia
  • Childhood volvulus
  • Cln1 disease
  • Cln3 disease
  • Cln5 disease
  • Cockayne syndrome type 2
  • Cold induced sweating syndrome
  • Coloboma of eye lens
  • Congenital afibrinogenemia
  • Congenital aplastic anemia
  • Congenital contractures
  • Congenital femoral deficiency
  • Congenital fiber type disproportion
  • Congenital fibrinogen deficiency
  • Congenital generalized fibromatosis
  • Congenital hemolytic anemia
  • Congenital herpes simplex
  • Congenital lipoid adrenal hyperplasia
  • Congenital microcoria
  • Congenital mitral stenosis
  • Congenital mumps
  • Congenital muscular dystrophy type 1a
  • Congenital nonhemolytic jaundice
  • Congenital plasminogen deficiency
  • Congenital pulmonary lymphangiectasia
  • Cranioectodermal dysplasia
  • Craniofacial deafness hand syndrome
  • Cryptosporidium enteritis
  • Curry jones syndrome
  • Cystic adenomatoid malformation of lung
  • Cytochrome p450 oxidoreductase deficiency
  • Cytoplasmic body myopathy
  • Dehydrated hereditary stomatocytosis
  • Desbuquois syndrome
  • Developmental expressive language disorder
  • Developmental reading disorder
  • Diffuse mesangial sclerosis
  • Dihydropteridine reductase deficiency
  • Distal 18q deletion syndrome
  • Encephalocele anencephaly
  • Epilepsy with myoclonic atonic seizures
  • Exstrophy epispadias complex
  • Familial glucocorticoid deficiency
  • Familial hypopituitarism
  • Familial paroxysmal nonkinesigenic dyskinesia
  • Familial porencephaly
  • Farber lipogranulomatosis
  • Fetal akinesia sequence
  • Fetal and neonatal alloimmune thrombocytopenia
  • Fetal edema
  • Fetal thalidomide syndrome
  • Filippi syndrome
  • Fountain syndrome
  • Frank ter haar syndrome
  • Galactose epimerase deficiency
  • Gemss syndrome
  • Genetic epilepsy with febrile seizures plus
  • Genital dwarfism
  • Gorlin chaudhry moss syndrome
  • Hardikar syndrome
  • Hemangioma thrombocytopenia syndrome
  • Hemophilia a or b
  • Hereditary hypophosphatemic rickets
  • High blood pressure in infants
  • Histidinemia
  • Homocystinuria due to mthfr deficiency
  • Horizontal gaze palsy with progressive scoliosis
  • Hydrocephalus due to congenital stenosis of aqueduct of sylvius
  • Hygroma cervical
  • Hyperlysinemia
  • Hypochondrogenesis
  • Inborn amino acid metabolism disorder
  • Increased head circumference
  • Infant hyperglycemia
  • Infantile onset spinocerebellar ataxia
  • Isolated growth hormone deficiency
  • Microcephalic osteodysplastic primordial dwarfism type 1
  • Microcephalic osteodysplastic primordial dwarfism type 2
  • Mucolipidosis 3
  • Mucopolysaccharidosis type 3a
  • Mucopolysaccharidosis type 3b
  • Mucopolysaccharidosis type 4
  • Mucopolysaccharidosis type 4a
  • Mucopolysaccharidosis type 6
  • Mucopolysaccharidosis type 7
  • Mulibrey nanism
  • Neonatal ovarian cyst
  • Neonatal severe hyperparathyroidism
  • Nonbullous congenital ichthyosiform erythroderma
  • Oculocerebrocutaneous syndrome
  • Omphalomesenteric cyst
  • Oppenheim dystonia
  • Ornithine translocase deficiency
  • Orofaciodigital syndrome 1
  • Orotic aciduria type 1
  • Overhydrated hereditary stomatocytosis
  • Palatopharyngeal incompetence
  • Paris trousseau thrombocytopenia
  • Partial atrioventricular canal
  • Pena shokeir syndrome type 2
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Phacomatosis pigmentokeratotica
  • Phacomatosis pigmentovascularis
  • Phosphoglycerate kinase deficiency
  • Phosphoglycerate mutase deficiency
  • Pmm2 congenital disorder of glycosylation
  • Potassium aggravated myotonia
  • Primary intestinal lymphangiectasia
  • Pulmonary atresia with ventricular septal defect
  • Rubella or measles
  • Toriello carey syndrome
  • Transient neonatal diabetes mellitus
  • Trisomy 12 mosaicism
  • Trisomy 17 mosaicism
  • Trisomy 3 mosaicism
  • Walker dyson syndrome
  • X linked creatine deficiency
  • X linked infantile spinal muscular atrophy
  • X linked intellectual disability
  • X linked severe combined immunodeficiency
  • Yunis varon syndrome
  • Ulcers
  • Primary immunodeficiency
  • Monkeypox
more..
Treatments & Procedures
  • Pediatric urgent care
  • Vaccines
  • Circumcision
  • Ear tubes
  • Well child visits
  • Immunization
  • Ear wax removal
  • X ray
  • Allergy testing
  • Blood tests
  • Bone density test
  • Clinical trials
  • Dexa scan
  • Immunizations
  • Physical examination
  • Smoking cessation
  • Staple removal
  • Annual wellness exam
  • Blood glucose monitoring
  • Lumbar puncture
  • Blood pressure medication
  • Cancer screening
  • Care coordination
  • Chronic care management
  • Pediatric laproscopy
  • Pediatric thoracoscopy
  • Medical ear piercing
  • Tetralogy of fallot repair
  • Tof repair
  • Pediatric sleep problems
  • Prematurity and low birth weight
  • Dental exams and cleanings
  • Semaglutide
more..
Additional Services
  • COVID-19 Testing

Frequently Asked Questions

Where is Snoqualmie Valley Hospital located?

Snoqualmie Valley Hospital is located in 35020 Southeast Kinsey Street Snoqualmie, WA 98065.

What are the various modes of payment does Snoqualmie Valley Hospital Accept?

Snoqualmie Valley Hospital accepts Card | Cash.

What are the doctors who practice in Snoqualmie Valley Hospital specialize in?

Currently there are around 4 providers practice in Snoqualmie Valley Hospital who specialise in DPC Family Medicine and Concierge Pediatrics, etc

How can I make appointments with doctors in Snoqualmie Valley Hospital?

You can take appointments for doctors who practice in Snoqualmie Valley Hospital online on their website or by calling them.

Location