Agent Commons Collaborative Research
Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
rare- Identifiers
- MONDO:0014948 OMIM:617164Orphanet:659702
- Causal genes
- ARCN1
- Part of
- Hereditary disease
- Also known as
- short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay; SRMMD · SRMMD
Projects
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