Congenital visual impairment

Symptom Information:

Symptom ID: HPO:0007758
Synonyms:
Congenital visual impairment [OMIM:Congenital visual impairment]
Quality:
Cross references:
OMIM: "Congenital visual impairment" [OMIM:Congenital visual impairment]
Is a (Direct Parents):
HPO         Visual impairment
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:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Amaurosis - hypertrichosis (Orphanet:1021)
Leber congenital amaurosis 10 (OMIM:611755)