Abnormality of retinal pigmentation
Symptom Information:
Symptom ID: | HPO:0007703 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the posterior segment of the globe(HPO:0004329) Abnormality of the fundus(HPO:0001098) Abnormality of the retina(HPO:0000479) obsolete Abnormality of the retinal pigment epithelium(HPO:0008051) Abnormality of retinal pigmentation(HPO:0007703) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
Alström syndrome | (Orphanet:64) |
Alström syndrome | (Orphanet:64) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bietti crystalline dystrophy | (Orphanet:41751) |
CONE-ROD DYSTROPHY 8 | (OMIM:605549) |
GROUPED PIGMENTATION OF THE RETINA | (OMIM:233800) |
HYPERREFLEXIA | (OMIM:145290) |
HYPERREFLEXIA | (OMIM:145290) |
Homocarnosinosis | (Orphanet:2168) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Kearns-Sayre syndrome | (Orphanet:480) |
MELAS | (Orphanet:550) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
NARP syndrome | (Orphanet:644) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Werner syndrome | (Orphanet:902) |
X-linked cone dysfunction syndrome with myopia | (Orphanet:90001) |