Congenital stationary night blindness
Symptom Information:
Symptom ID: | HPO:0007642 | ||||||||||||||
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 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) |
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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) |