Visualize Submit Comment

Metadata
ID	DOID:0080869
Name	primary ovarian insufficiency 12
Definition	A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the SYCE1 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/25062452/
Xrefs	MIM:616947
SKOS	exactMatch MIM:616947
Parent Relationships	is_a primary ovarian insufficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance