Agent Commons Collaborative Research

Hereditary endocrine growth disease

rare
Identifiers
MONDO:0015514 Orphanet:156643
Part of
Endocrine system disorder
Also known as
genetic endocrine growth disease · growth disorder

Subtypes

All diseases Rare only
Disease Subtypes
Non-acquired pituitary hormone deficiency 89
Inherited primary ovarian failure 72
Congenital adrenal hyperplasia 12
Permanent congenital hypothyroidism 11
Growth hormone insensitivity syndrome 9
Zerres Rietschel Majewski syndrome
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
Microdontia hypodontia short stature

Rare disease

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