Congenital stationary night blindness

Symptom Information:

Symptom ID: HPO:0007642
Synonyms:
Complete congenital stationary night blindness [HPO:0007642]
Congenital night blindness [HPO:0007642]
NIGHT BLINDNESS, CONGENITAL [HPO:0007642]
NIGHT BLINDNESS, CONGENITAL STATIONARY [HPO:0007642]
NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE [HPO:0007642]
NIGHT BLINDNESS, STATIONARY [HPO:0007642]
Static congenital hemeralopia [HPO:0007642]
Congenital night blindness [OMIM:Congenital night blindness]
Congenital stationary night blindness [OMIM:Congenital stationary night blindness]
Night blindness, congenital [OMIM:Night blindness, congenital]
Night blindness, congenital stationary [OMIM:Night blindness, congenital stationary]
Night blindness, congenital stationary, complete [OMIM:Night blindness, congenital stationary, complete]
Night blindness, stationary [OMIM:Night blindness, stationary]
Congenital night blindness [MedDRA:10010559]
Quality:
Cross references:
OMIM: "Congenital night blindness" [OMIM:Congenital night blindness]
OMIM: "Congenital stationary night blindness" [OMIM:Congenital stationary night blindness]
OMIM: "Night blindness, congenital" [OMIM:Night blindness, congenital]
OMIM: "Night blindness, congenital stationary" [OMIM:Night blindness, congenital stationary]
OMIM: "Night blindness, congenital stationary, complete" [OMIM:Night blindness, congenital stationary, complete]
OMIM: "Night blindness, stationary" [OMIM:Night blindness, stationary]
Is a (Direct Parents):
MedDRA Retinal disorders congenital
HPO         Nyctalopia
HPO         Congenital stationary night blindness with normal fundus
HPO         Congenital stationary night blindness with abnormal fundus
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)
                Nyctalopia(HPO:0000662)
                   Congenital stationary night blindness(HPO:0007642)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Retinal disorders congenital(MedDRA:10038855)
          Congenital stationary night blindness(HPO:0007642)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Congenital stationary night blindness (Orphanet:215)
DEAFNESS, AUTOSOMAL RECESSIVE 37 (OMIM:607821)
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1 (OMIM:610445)
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2 (OMIM:163500)
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3 (OMIM:610444)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A (OMIM:310500)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B (OMIM:257270)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D (OMIM:613830)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E (OMIM:614565)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F (OMIM:615058)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A (OMIM:300071)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (OMIM:610427)
OGUCHI DISEASE 1 (OMIM:258100)
OGUCHI DISEASE 2 (OMIM:613411)
Oguchi disease (Orphanet:75382)