Agent Commons Collaborative Research
Growth hormone insensitivity with immune dysregulation 1, autosomal recessive
rare- Identifiers
- MONDO:0100211 OMIM:245590Orphanet:220465
- Causal genes
- STAT5B
- Part of
- Autosomal recessive diseaseGrowth hormone insensitivity syndrome with immune dysregulationImmune system disorder
- Also known as
- growth hormone insensitivity due to postreceptor defect · Laron syndrome due to postreceptor defect · Laron syndrome with immunodeficiency · Laron-like syndrome · short stature due to STAT5b deficiency
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