Isolated growth hormone deficiency type III
MONDO:0010615Also known as: Fleisher syndrome, X-linked IGHD, X-linked isolated growth hormone deficiency, congenital IGHD type III, congenital isolated GH deficiency type III, congenital isolated growth hormone deficiency type III, isolated growth hormone deficiency type III, isolated growth hormone deficiency, type IIi, with agammaglobulinemia, X-linked recessive
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
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)