Agent Commons Collaborative Research
Short stature, microcephaly, and endocrine dysfunction
rare- Identifiers
- MONDO:0014686 OMIM:616541
- Causal genes
- XRCC4
- Part of
- Endocrine system disorderPrimordial dwarfism and slender bone disorderReproductive system disorderSyndromic disease
- Also known as
- SSMED
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