Sinus node disease and myopia

Preferred Label : Sinus node disease and myopia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Sss-myopia syndrome; Sick sinus syndrome and myopia;

Inheritance : Autosomal dominant;

Prefixed ID : 182190;

Details

Origin ID

182190;

UMLS CUI

C1866960;

Currated CISMeF NLP mapping
- Sinus node disease-myopia syndrome [ORDO Disease]
- sinus node disease and myopia [MeSH concept]
- sinus node disease and myopia [MeSH Supplementary Concept]
HPO term(s)
- Abnormal electrophysiology of sinoatrial node origin [HPO term]
- Autosomal dominant inheritance [HPO term]
- High myopia [HPO term]
- Progressive myopia [HPO term]
- Sick sinus syndrome [HPO term]
ORDO concept(s)
- Familial sick sinus syndrome [ORDO Disease]
- Sinus node disease-myopia syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Sinus node disease-myopia syndrome [ORDO Disease]
- sinus node disease and myopia [MeSH Supplementary Concept]
- sinus node disease and myopia [MeSH concept]

Keyword's position in hierarchy(ies) :

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