Endocrine Diseases | Page 2

269 diseases found in 3 pages

F Diseases

Frasier syndrome

G Diseases

Galactokinase deficiency Genito palato cardiac syndrome Gigantism Glucocorticoid-remediable aldosteronism Goblet cell carcinoid Granulomatous hypophysitis Graves disease Growth hormone deficiency

H Diseases

Hepatic lipase deficiency Hereditary diffuse gastric cancer Hereditary hyperekplexia Hereditary pancreatitis Hereditary paraganglioma-pheochromocytoma Histiocytosis-lymphadenopathy plus syndrome Holoprosencephaly Hydrocephalus obesity hypogonadism Hyperadrenalism Hyperinsulinism due to glucokinase deficiency Hyperinsulinism-hyperammonemia syndrome Hyperlipidemia type 3 Hyperlipoproteinemia type 5 Hyperparathyroidism-jaw tumor syndrome Hypocalcemia, autosomal dominant Hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia Hypoparathyroidism Hypoparathyroidism-intellectual disability-dysmorphism syndrome Hypophosphatemic rickets Hypopituitarism

I Diseases

IMAGe syndrome Immunodysregulation, polyendocrinopathy and enteropathy X-linked Insulin-like growth factor 1 resistance to Insulin-like growth factor I deficiency Insulin-resistance type B Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity Iodine antenatal exposure Isolated ACTH deficiency Isolated growth hormone deficiency type 1A Isolated growth hormone deficiency type 3

J Diseases

Johanson-Blizzard syndrome

K Diseases

Kallmann syndrome Kallmann syndrome 1 Kearns-Sayre syndrome Kenny-Caffey syndrome type 1 Kenny-Caffey syndrome type 2 Kowarski syndrome

L Diseases

Langerhans cell histiocytosis Laron syndrome Laurence-Moon syndrome LCHAD deficiency Leprechaunism Li-Fraumeni syndrome LIPE-related familial partial lipodystrophy Lipodystrophy, familial partial, type 5 LRBA deficiency Lubinsky syndrome

M Diseases

Male pseudohermaphroditism intellectual disability syndrome, Verloes type Mandibuloacral dysplasia with type A lipodystrophy Mandibuloacral dysplasia with type B lipodystrophy Martsolf syndrome Maternally inherited diabetes and deafness Maturity-onset diabetes of the young Maturity-onset diabetes of the young, type 1 Maturity-onset diabetes of the young, type 2 Maturity-onset diabetes of the young, type 3 Maturity-onset diabetes of the young, type 4 Maturity-onset diabetes of the young, type 5 Maturity-onset diabetes of the young, type 6 Maturity-onset diabetes of the young, type 7 Maturity-onset diabetes of the young, type 8 Maturity-onset diabetes of the young, type 9 McCune-Albright syndrome Meacham Winn Culler syndrome Meningioma Merkel cell carcinoma Microcephalic osteodysplastic primordial dwarfism type 2 Mitochondrial myopathy with diabetes MOMO syndrome Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Myotonic dystrophy type 1 Myotonic dystrophy type 2

N Diseases

Neonatal adrenoleukodystrophy Neonatal progeroid syndrome Neonatal severe hyperparathyroidism Noonan syndrome Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6

O Diseases

Obesity due to congenital leptin deficiency Optic pathway glioma Ovarian small cell carcinoma

P Diseases

PAGOD syndrome Pallister-Hall syndrome Panhypopituitarism X-linked

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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