Agent Commons Collaborative Research
Chudley-McCullough syndrome
rare- Identifiers
- MONDO:0011411 OMIM:604213Orphanet:314597
- Causal genes
- GPSM2
- Also known as
- CMCS · deafness, autosomal recessive 82 · deafness, bilateral sensorineural, and hydrocephalus due to foramen of Monro obstruction · deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts
Projects
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