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Cone-Rod Dystrophy 19

Disease ID: disease_node_16582

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DbxrefMIM:615860
SubclassofDOID_0050572
Data SourceDOID
SynonymsCORD19
Doid Labelcone-rod dystrophy 19
Doid DescriptionA cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the TTLL5 gene on chromosome 14q24.
Disease Node Iddisease_node_16582
Doid IdDOID_0111025
LabelCone-Rod Dystrophy 19