Hypopigmented fundi
Symptom Information:
Symptom ID: | HPO:0001487 | |||
Synonyms: |
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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) Hypopigmented fundi(HPO:0001487) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Retinitis pigmentosa 10 | (OMIM:180105) |
Tietz syndrome | (Orphanet:42665) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Ă…land Islands eye disease | (Orphanet:178333) |