clinic

Ethos Endocrinology

5 Stars (10 Reviews)

Ethos Endocrinology is a clinic that specializes in Concierge Endocrinology. The clinic is located in Houston, Texas. Ethos Endocrinology is known for housing expert physicians. Ethos Endocrinology offers all the services, treatments and procedures pertinent to the specialties mentioned above.

1 Doctor | Website
Overview
Providers
Reviews
Services
Location
About Ethos Endocrinology

"Ethos Endocrinology restores the sacred bond of the patient-doctor relationship. We do that by employing a direct care model.After completing his residency and fellowship training at the highly-ranked Baylor College of Medicine in the Texas Medical Center, Dr. Kanji designed a health care experience to restore the patient-doctor relationship. How?

First, eliminate interference from insurance. Second, limit the number of members to maximize your time and experience. Third, keep it affordable. The result is Ethos Endocrinology."

Address

2500 Fondren Road Suite 320, Houston,
TX 77085

Modes of Payment

Card | Cash

Providers
Aleem Kanji - 2500 Fondren Road, Houston, Texas, 77085
Aleem Kanji, MD
Ethos Endocrinology
Concierge Endocrinology
(10)
Fee $101 - $250
Max no. of Patients: N/A
Accepting New Patients: NA
2500 Fondren Road, Suite 320, Houston, TX 77085
Message
Call
Website
Reviews
Posted by FMDD User
December 19, 2023

Review For Aleem Kanji

Posted by FMDD User
December 10, 2023

Review For Aleem Kanji

Posted by FMDD User
January 16, 2024

Review For Aleem Kanji

Posted by FMDD User
January 23, 2024

Review For Aleem Kanji

Conditions Treated
  • Adenomyosis
  • Thyroid cancer
  • Thyroid eye disease
  • Uterine fibroids
  • Osteoporosis
  • Ectopic pregnancy
  • Ovarian cysts
  • Obesity
  • Diabetes
  • Gestational diabetes
  • Atherosclerosis
  • Diabetic ketoacidosis
  • Addison's disease
  • Endometriosis
  • Hypothyroidism
  • Hyperthyroidism
  • Type 2 diabetes
  • Type 1 diabetes
  • Cushing syndrome
  • Graves' disease
  • Acromegaly
  • Androgen insensitivity syndrome
  • Apoplexy
  • Carcinoid syndrome
  • Congenital adrenal hyperplasia
  • Diabetes insipidus
  • Diabetes mellitus
  • Diabetic foot ulcers
  • Diabetic neuropathy
  • Diabetic retinopathy
  • Familial hypercholesterolemia
  • Fibrous dysplasia
  • Gigantism
  • Growth hormone deficiency
  • Hashimoto thyroiditis
  • High potassium level
  • Hyperaldosteronism
  • Hypercalcemia
  • Hyperparathyroidism
  • Hypogonadism
  • Hypoparathyroidism
  • Hypophosphatemia
  • Hypopituitarism
  • Kallmann syndrome
  • Low blood sugar
  • Low testosterone
  • Macrosomia
  • Magnesium deficiency
  • Malnutrition
  • Metabolic acidosis
  • Metabolic syndrome
  • Neuroendocrine tumor
  • Non alcoholic fatty liver disease
  • Noonan syndrome
  • Osteomalacia
  • Ovarian hyperstimulation syndrome
  • Papillary thyroid cancer
  • Phenylketonuria
  • Pheochromocytoma
  • Pituitary tumor
  • Precocious puberty
  • Prolactinoma
  • Rickets
  • Thyroid nodule
  • Thyroid storm
  • Thyroiditis
  • Xanthoma
  • Zollinger ellison syndrome
  • Abetalipoproteinemia
  • Adrenal cancer
  • Adrenal gland adenoma
  • Adrenocortical carcinoma
  • Albright's hereditary osteodystrophy
  • Alcoholic ketoacidosis
  • Alkaptonuria
  • Alstrom syndrome
  • Anaplastic thyroid cancer
  • Bardet biedl syndrome
  • Bartter syndrome
  • Congenital hyperinsulinism
  • Congenital hypothyroidism
  • Diabetic foot care
  • Diabetic macular edema
  • Diabetic nephropathy
  • Diabetic peripheral neuropathy
  • Empty sella syndrome
  • Female pattern baldness
  • Floating harbor syndrome
  • Follicular cyst of the ovary
  • Follicular thyroid cancer
  • Gitelman syndrome
  • Glucagonoma
  • Gonadal dysgenesis
  • Hirsutism in women
  • Hypervitaminosis d
  • Hypoaldosteronism
  • Hypogonadotropic hypogonadism
  • Insulinoma
  • Laron syndrome
  • Liddle syndrome
  • Low potassium level
  • Male infertility
  • Mccune albright syndrome
  • Medullary thyroid carcinoma
  • Milk alkali syndrome
  • Multiple endocrine neoplasia
  • Multiple endocrine neoplasia type 2
  • Nelson syndrome
  • Nephrocalcinosis
  • Nephrogenic diabetes insipidus
  • Newborn low blood sugar
  • Ornithine transcarbamylase deficiency
  • Panhypopituitarism
  • Parathyroid adenoma
  • Parathyroid cancer
  • Pituitary apoplexy
  • Pituitary dwarfism
  • Premature ovarian failure
  • Pseudohypoparathyroidism
  • Renal glycosuria
  • Secondary adrenal insufficiency
  • Short stature
  • Subacute thyroiditis
  • Swyer syndrome
  • Syndrome of inappropriate antidiuretic hormone secretion
  • Thyroid disorders
  • Weight management
  • Wolfram syndrome
  • Acute adrenal crisis
  • Apparent mineralocorticoid excess
  • Aromatase deficiency
  • Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
  • Autoimmune polyglandular syndrome type 2
  • Breast enlargement in males
  • Delayed growth
  • Disorders of lipoid metabolism
  • Donohue syndrome
  • Ectopic cushing syndrome
  • Endocrinology and metabolism
  • Exogenous cushing syndrome
  • Familial combined hyperlipidemia
  • Familial hypertriglyceridemia
  • Familial hypobetalipoproteinemia
  • Familial partial lipodystrophy
  • Fanconi bickel syndrome
  • Female infertility
  • Galactokinase deficiency
  • Glucocorticoid remediable aldosteronism
  • Glucocorticoid resistance
  • Glycogen storage disease type 0
  • Glycogen storage disease type 3
  • Heterozygous familial hypercholesterolemia
  • Homozygous familial hypercholesterolemia
  • Hypoglycemic coma
  • Hypothalamic tumor
  • Idiopathic hypercalciuria
  • Leydig cell hypoplasia
  • Maturity onset diabetes of the young
  • Molybdenum cofactor deficiency
  • Multiple endocrine neoplasia type 1
  • Multiple symmetric lipomatosis
  • Neonatal hypothyroidism
  • Non toxic goiter
  • Osteitis fibrosa
  • Ovarian dysfunction
  • Overweight and obesity
  • Parathyroid hyperplasia
  • Partial androgen insensitivity syndrome
  • Pediatric obesity
  • Persistent mullerian duct syndrome
  • Pinealectomy
  • Primary angle closure glaucoma
  • Progressive osseous heteroplasia
  • Pseudohypoaldosteronism type 1
  • Puberty disorder
  • Pyruvate dehydrogenase deficiency
  • Rabson mendenhall syndrome
  • Russell silver dwarfism
  • Shapiro syndrome
  • Short chain acyl coa dehydrogenase deficiency
  • Short syndrome
  • Silent thyroiditis
  • Sitosterolemia
  • Somatostatinoma
  • Testicular failure
  • Thyroid dysgenesis
  • Thyrotoxic periodic paralysis
  • Toxic nodular goiter
  • Triple a syndrome
  • Very long chain acyl coa dehydrogenase deficiency
  • Wolcott rallison syndrome
  • Abdominal obesity metabolic syndrome
  • Acromegaloid facial appearance syndrome
  • Autosomal dominant hypocalcemia
  • Benign thyroid diseases
  • Carnitine acylcarnitine translocase deficiency
  • Carnitine palmitoyltransferase 1 deficiency
  • Childhood hypophosphatasia
  • Cold induced sweating syndrome
  • Congenital lipoid adrenal hyperplasia
  • Cushing syndrome due to adrenal tumor
  • Cytochrome p450 oxidoreductase deficiency
  • Diabetic hyperglycemic hyperosmolar syndrome
  • Diabetic kidney disorder
  • Essential pentosuria
  • Familial glucocorticoid deficiency
  • Familial hdl deficiency
  • Familial hyperaldosteronism
  • Familial hypertension
  • Familial hypopituitarism
  • Familial isolated hyperparathyroidism
  • Familial lipoprotein lipase deficiency
  • Fertility and conception
  • Fructose 1
  • Generalized resistance to thyroid hormone
  • Genital dwarfism
  • Glucose transporter deficiency
  • Granulomatous hypophysitis
  • Hereditary hypophosphatemic rickets
  • Hereditary paraganglioma pheochromocytoma syndrome
  • Hyperglycerolemia
  • Hyperlipidemia type 3
  • Hyperlipoproteinemia type 4
  • Hyperlipoproteinemia type 5
  • Hypolipoproteinemia
  • Infant hyperglycemia
  • Isolated acth deficiency
  • Isolated growth hormone deficiency
  • Isolated hypogonadotropic hypogonadism
  • Kenny caffey syndrome type 2
  • Long chain 3 hydroxyacyl coa dehydrogenase deficiency
  • Malonyl coa decarboxylase deficiency
  • Maternal hyperphenylalaninemia
  • Menopausal and postmenopausal disorders
  • Metastatic insulinoma
  • Methylmalonic acidemia with homocystinuria
  • Morgagni stewart morel syndrome
  • Multiple carboxylase deficiency
  • Neonatal severe hyperparathyroidism
  • Neurohypophyseal diabetes insipidus
  • Ornithine translocase deficiency
  • Osteoporosis pseudoglioma syndrome
  • Ovarian overproduction of androgens
  • Peroxisomal acyl coa oxidase deficiency
  • Pgm1 cdg
  • Pmm2 congenital disorder of glycosylation
  • Pseudohypoaldosteronism type 2
  • Rft1 cdg
  • Thyroid hormone plasma membrane transport defect
  • Transient neonatal diabetes mellitus
  • Type a insulin resistance syndrome
  • Type b insulin resistance syndrome
  • Weight control and obesity
more..
Treatments & Procedures
  • Hormone replacement therapy
  • Dexa scan
  • Bone density test
  • Blood glucose monitoring
  • Insulin treatment
  • Bone densitometry
  • Hormone treatments
  • Dietary counseling
  • Point of care a1c

Frequently Asked Questions

Where is Ethos Endocrinology located?

Ethos Endocrinology is located in 2500 Fondren Road Suite 320, Houston, TX 77085.

What are the various modes of payment does Ethos Endocrinology Accept?

Ethos Endocrinology accepts Card | Cash.

What are the doctors who practice in Ethos Endocrinology specialize in?

Currently there are around 1 providers practice in Ethos Endocrinology who specialise in Concierge Endocrinology, etc

How can I make appointments with doctors in Ethos Endocrinology?

You can take appointments for doctors who practice in Ethos Endocrinology online on their website or by calling them.

Location