Isolated growth hormone deficiency type IB
MONDO:0013006An 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.
Also known as: congenital IGHD type IB, congenital isolated GH deficiency type IB, congenital isolated growth hormone deficiency type IB, dwarfism of Sindh, growth hormone deficiency, isolated, type IB, IGHD 1B, IGHD1B, isolated Growth hormone deficiency, type 1B
9 clinical trials for this condition and its sub-types.
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Brain disorder
(110)
Central nervous system disorder
(97)
Endocrine system disorder
(61)
Hypogonadism
(41)
Isolated congenital growth hormone deficiency
(29)
Hereditary endocrine growth disease
(23)
Hypogonadotropic hypogonadism
(15)