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Metadata
ID DOID:0060872
Name isolated growth hormone deficiency type II
Definition An isolated growth hormone deficiency characterized by autosomal dominant inheritance of low but detectable levels of GH1 resulting in variable degrees of dwarfism which are responsive to growth hormone therapy that has_material_basis_in dominant negative mutations in the GH1 gene on chromosome 17q23.3.
https://www.ncbi.nlm.nih.gov/pubmed/15671105, https://www.ncbi.nlm.nih.gov/pubmed/8288694
Xrefs

ICD10CM:E23.0

MESH:C562704

MIM:173100

ORDO:231679

Subsets

DO_rare_slim

Synonyms

autosomal dominant isolated growth hormone deficiency [EXACT]

autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency [EXACT]

congenital IGHD type II [EXACT]

congenital isolated GH deficiency type II [EXACT]

congenital isolated growth hormone deficiency type II [EXACT]

IGHD II [EXACT]

Parent Relationships

is_a isolated growth hormone deficiency

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