Congenital nystagmus
Symptom Information:
Symptom ID: | HPO:0006934 | ||||
Synonyms: |
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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 eye movement(HPO:0000496) Abnormal involuntary eye movements(HPO:0012547) Nystagmus(HPO:0000639) Congenital nystagmus(HPO:0006934) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Coordination and balance disturbances(MedDRA:10072984) Congenital nystagmus(HPO:0006934) |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aplasia cutis - myopia | (Orphanet:1117) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Diabetic embryopathy | (Orphanet:1926) |
Foveal hypoplasia - presenile cataract | (Orphanet:2253) |
Hermansky-Pudlak syndrome type 9 | (Orphanet:280663) |
Karsch-Neugebauer syndrome | (Orphanet:2329) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
NYSTAGMUS 1, CONGENITAL, X-LINKED | (OMIM:310700) |
NYSTAGMUS, CONGENITAL, AUTOSOMAL RECESSIVE | (OMIM:257400) |