Search Ontology:
Human Disease

Ritscher-Schinzel syndrome 2

Term ID
DOID:0060572
Synonyms
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
Ontology
Human Disease   ( DOID:0060572 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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