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Up to: Isolated congenital growth hormone deficiency
Isolated growth hormone deficiency type IA
An isolated growth hormone deficiency characterized by autosomal recessive inheritance of severe dwarfism with onset by 6 months of age and variable development of antibodies to growth hormone following exogenous supplementation that has material basis in null mutations in the GH1 gene on chromosome 17q23.3.
This condition has no sub-types.