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Isolated congenital growth hormone deficiency

rare

Identifiers: MONDO:0000050 Orphanet:631
Part of: Combined pituitary hormone deficiencies, genetic form
Also known as: congenital IGHD · congenital isolated GH deficiency · congenital isolated growth hormone deficiency · ICGHD · isolated growth hormone deficiency

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Isolated growth hormone deficiency type III	MONDO:0010615	1	BTK
Isolated growth hormone deficiency type IA	MONDO:0009876		GH1
Isolated growth hormone deficiency type IB	MONDO:0013006		GH1
Isolated growth hormone deficiency type II	MONDO:0008250		GH1
Isolated growth hormone deficiency, type 4	MONDO:0032567		GHRHR
Isolated growth hormone deficiency, type 5	MONDO:0032569		RNPC3
Short stature due to growth hormone qualitative anomaly	MONDO:0009879		GH1

Rare disease

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