Nystagmus 5, congenital, X-linked

Preferred Label : Nystagmus 5, congenital, X-linked;

Symbol : NYS5;

CISMeF acronym : NYS5;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of congenital nystagmus, see NYS1 (310700).;

Inheritance : X-linked dominant;

Prefixed ID : %300589;

Details

Origin ID

300589;

UMLS CUI

C1845116;

Currated CISMeF NLP mapping
- nystagmus 5, infantile periodic alternating [MeSH Supplementary Concept]
DO Cross reference
- congenital nystagmus 5 [DO Concept]
HPO term(s)
- Abnormal stereopsis [HPO term]
- Hyperopic astigmatism [HPO term]
- Nystagmus [HPO term]
- Strabismus [HPO term]
- X-linked dominant inheritance [HPO term]
ORDO concept(s)
- Congenital idiopathic nystagmus [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- nystagmus 5, infantile periodic alternating [MeSH Supplementary Concept]
- nystagmus 5, infantile periodic alternating [MeSH concept]
Validated automatic mappings to NTBT
- Congenital idiopathic nystagmus [ORDO Disease]

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