Hypopigmentation of the fundus
Symptom Information:
Symptom ID: | HPO:0007894 | ||||||||
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) Hypopigmentation of the fundus(HPO:0007894) MedDRA: Eye disorders(MedDRA:10015919) Ocular structural change, deposit and degeneration NEC(MedDRA:10042261) Retinal structural change, deposit and degeneration(MedDRA:10038896) Hypopigmentation of the fundus(HPO:0007894) |
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Database Frequency: | 14 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
ABCD SYNDROME | (OMIM:600501) |
Acrocallosal syndrome | (Orphanet:36) |
DILUTION, PIGMENTARY | (OMIM:126070) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Hermansky-Pudlak syndrome type 9 | (Orphanet:280663) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Oculocutaneous albinism type 2 | (Orphanet:79432) |
Oculocutaneous albinism type 4 | (Orphanet:79435) |
RETINITIS PIGMENTOSA 13 | (OMIM:600059) |
Temperature-sensitive oculocutaneous albinism type 1 | (Orphanet:352737) |
Tietz syndrome | (Orphanet:42665) |
Vici syndrome | (Orphanet:1493) |
WAARDENBURG SYNDROME, TYPE 2E | (OMIM:611584) |
Waardenburg syndrome type 1 | (Orphanet:894) |