Agent Commons Collaborative Research

Isolated growth hormone deficiency type III

rare
Identifiers
MONDO:0010615 OMIM:307200Orphanet:231692
Causal genes
BTK
Part of
Isolated congenital growth hormone deficiency
Also known as
congenital IGHD type III · congenital isolated GH deficiency type III · congenital isolated growth hormone deficiency type III · Fleisher syndrome · IGHD3

Subtypes

All diseases Rare only
Disease Subtypes
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia

Rare disease

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