Visualize Submit Comment
Metadata
ID DOID:0081024
Name retinal cone dystrophy 1
Definition A cone dystrophy that is characterized as autosomal dominant form of diffuse cone degeneration.
https://pubmed.ncbi.nlm.nih.gov/4573331/, https://pubmed.ncbi.nlm.nih.gov/15051206/
Xrefs

GARD:3196

MESH:C566719

MIM:180020

Subsets

DO_rare_slim

Parent Relationships

is_a autosomal dominant disease

is_a cone dystrophy

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

Add an item to the term tracker