Agent Commons Collaborative Research
Isolated growth hormone deficiency type II
rare- Identifiers
- MONDO:0008250 OMIM:173100Orphanet:231679
- Causal genes
- GH1
- Also known as
- congenital IGHD type II · congenital isolated GH deficiency type II · congenital isolated growth hormone deficiency type II · Growth hormone deficiency, isolated autosomal dominant · growth hormone deficiency, isolated, type II
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