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Metadata
ID	DOID:0070354
Name	cataract 48
Definition	A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment. https://www.ncbi.nlm.nih.gov/pubmed/30290152, https://www.omim.org/entry/618415
Xrefs	MIM:618415
Synonyms	CTRCT48 [EXACT]
Parent Relationships	is_a cataract is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance