Search Ontology:
Human Disease

cone-rod dystrophy 21

Term ID
DOID:0081447
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0081447 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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