Nystagmus 3, congenital, autosomal dominant

Preferred Label : Nystagmus 3, congenital, autosomal dominant;

Symbol : NYS3;

CISMeF acronym : NYS3;

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 : Autosomal dominant;

Prefixed ID : %608345;

Details

Origin ID

608345;

UMLS CUI

C1842186;

Broader ORDO disease(s)
- Congenital idiopathic nystagmus [ORDO Disease]
Currated CISMeF NLP mapping
- Nystagmus 3, congenital, autosomal dominant [MeSH concept]
- nystagmus 3, congenital, autosomal dominant [MeSH Supplementary Concept]
DO Cross reference
- congenital nystagmus 3 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Heterogeneous [HPO term]
- Horizontal jerk nystagmus [HPO term]
- Subnormal visual acuity [HPO term]
Not associated HPO term(s)
- Visual impairment [HPO term]
ORDO concept(s)
- Congenital idiopathic nystagmus [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nystagmus 3, congenital, autosomal dominant [MeSH concept]
- nystagmus 3, congenital, autosomal dominant [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Congenital idiopathic nystagmus [ORDO Disease]

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