Search Ontology:
Human Disease
Coffin-Siris syndrome 5
- Term ID
- DOID:0112368
- Synonyms
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- CSS5
- Definition
- A Coffin-Siris syndrome characterized by delayed psychomotor development, intellectual disability, coarse facial features, and hypoplasia of the distal phalanges, particularly the fifth digit that has_material_basis_in heterozygous mutation in the SMARCE1 gene on chromosome 17q21.2. (2)
- References
- Ontology
- Human Disease ( DOID:0112368 )
- is a type of
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Genes Involved
Zebrafish Models