ZFIN Human Disease: cone dystrophy

OBO ID: DOID:0050795

Term Name:	cone dystrophy		Search Ontology:
Synonyms:	retinal cone dystrophy
Definition:	A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision. (3)
References:	GARD:11897 MESH:D000077765
Ontology:	Human Disease ( DOID:0050795 )

Relationships

is a type of:	retinal disease retinal disease Show first 5 Terms
has subtype:	retinal cone dystrophy 1 retinal cone dystrophy 3A retinal cone dystrophy 3B retinal cone dystrophy 4 retinal cone dystrophy 1 retinal cone dystrophy 3A retinal cone dystrophy 3B retinal cone dystrophy 4 Show first 5 Terms

OTHER cone dystrophy PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
WT	chemical treatment by injection: nucleic acid	Clark et al., 2019
cacna2d4a^zh5/zh5; cacna2d4b^zh6/zh6 (TU)	standard conditions	Schlegel et al., 2019

PHENOTYPE No data available

CITATIONS (4)