Optic nerve dysplasia

Symptom Information:

Symptom ID: HPO:0001093
Synonyms:
Optic nerve dysplasia [OMIM:Optic nerve dysplasia]
Quality:
Cross references:
OMIM: "Optic nerve dysplasia" [OMIM:Optic nerve dysplasia]
Is a (Direct Parents):
HPO         Abnormality of the optic nerve
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:
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)