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Metadata
ID	DOID:0081447
Name	cone-rod dystrophy 21
Definition	A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13. https://pubmed.ncbi.nlm.nih.gov/26720460/
Xrefs	MIM:616502
Parent Relationships	is_a cone-rod dystrophy is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance