Congenital blindness
Symptom Information:
Symptom ID: | HPO:0007875 | ||||
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 physiology(HPO:0012373) Abnormality of vision(HPO:0000504) Visual impairment(HPO:0000505) Blindness(HPO:0000618) Congenital blindness(HPO:0007875) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Eye disorders congenital(MedDRA:10015920) Ocular disorders congenital NEC(MedDRA:10027673) Congenital blindness(HPO:0007875) |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AICA-ribosiduria | (Orphanet:250977) |
Joubert syndrome 5 | (OMIM:610188) |
Leber congenital amaurosis | (Orphanet:65) |
Leber congenital amaurosis 12 | (OMIM:610612) |
Leber congenital amaurosis 14 | (OMIM:613341) |
POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS | (OMIM:263100) |
RETINAL APLASIA | (OMIM:179900) |
Senior-Loken syndrome 3 | (OMIM:606995) |
Senior-Loken syndrome 5 | (OMIM:609254) |