Search Ontology:
Human Disease

Ritscher-Schinzel syndrome 1

Term ID
DOID:0060571
Synonyms
Definition
A Ritscher-Schinzel syndrome that has_material_basis_in homozygous mutation in the KIAA0196 gene on chromosome 8q24. https://www.ncbi.nlm.nih.gov/pubmed/24065355
References
Ontology
Human Disease   ( DOID:0060571 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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