Congenital visual impairment
Symptom Information:
Symptom ID: | HPO:0007758 | ||
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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 physiology(HPO:0012373) Abnormality of vision(HPO:0000504) Visual impairment(HPO:0000505) Congenital visual impairment(HPO:0007758) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Amaurosis - hypertrichosis | (Orphanet:1021) |
Leber congenital amaurosis 10 | (OMIM:611755) |