OBO ID: DOID:0060572
Term Name: Ritscher-Schinzel syndrome 2 Search Ontology:
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 Ritscher-Schinzel syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CCDC22 Ritscher-Schinzel syndrome 2 300963
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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