Search Ontology:
Human Disease
Ritscher-Schinzel syndrome 2
- Term ID
- DOID:0060572
- Synonyms
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- Definition
- A Ritscher-Schinzel syndrome that has_material_basis_in mutation in the CCDC22 gene on chromosome Xp11. https://www.ncbi.nlm.nih.gov/pubmed/24916641
- References
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- OMIM:300963
- ORDO:7
- Ontology
- Human Disease ( DOID:0060572 )
- is a type of
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