Congenital blindness

Symptom Information:

Symptom ID: HPO:0007875
Synonyms:
Congenital amaurosis [HPO:0007875]
Congenital amaurosis [OMIM:Congenital amaurosis]
Congenital blindness [OMIM:Congenital blindness]
Blindness congenital [MedDRA:10005176]
Quality:
Cross references:
OMIM: "Congenital amaurosis" [OMIM:Congenital amaurosis]
OMIM: "Congenital blindness" [OMIM:Congenital blindness]
Is a (Direct Parents):
HPO         Blindness
MedDRA Ocular disorders congenital NEC
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)
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)