Optic nerve dysplasia
Symptom Information:
Symptom ID: | HPO:0001093 | ||
Synonyms: |
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Quality: | |||
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 optic nerve(HPO:0000587) Optic nerve dysplasia(HPO:0001093) MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Ocular albinism with congenital sensorineural deafness | (Orphanet:352740) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |