Visualize Submit Comment

Metadata
ID	DOID:0060572
Name	Ritscher-Schinzel syndrome 2
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
Xrefs	MIM:300963 ORDO:7
Subsets	DO_rare_slim
Parent Relationships	is_a Ritscher-Schinzel syndrome is_a X-linked recessive disease
Subclass Logical Relationships	has material basis in some X-linked recessive inheritance