An isolated growth hormone deficiency characterized by autosomal recessive inheritance of low but detectable levels of GH, short stature, significantly retarded bone age, and a positive response and immunologic tolerance to growth hormone therapy that has material basis in mutation in the GH1 or GHRHR genes on chromosomes 17q23.3 and 7p14.3, respectively.
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isolated growth hormone deficiency type II
MONDO:0008250
isolated growth hormone deficiency type IA
MONDO:0009876
short stature due to growth hormone qualitative anomaly
MONDO:0009879
isolated growth hormone deficiency type III
MONDO:0010615
isolated growth hormone deficiency, type 4
MONDO:0032567
isolated growth hormone deficiency, type 5
MONDO:0032569