Laryngeal adductor paralysis

Preferred Label : Laryngeal adductor paralysis;

Symbol : LAP;

CISMeF acronym : LAP;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Vocal cord dysfunction, adductor type;

Inheritance : Autosomal dominant;

Prefixed ID : %150270;

Details

Origin ID

150270;

UMLS CUI

C0396060;

Automatic exact mappings (from CISMeF team)
- ACP2 wt Allele [NCIt concept]
- CCAAT enhancer binding protein beta [HGNC gene]
- CEBPB wt Allele [NCIt concept]
- Lap [NCIt concept]
- Laryngeal abductor paralysis [ORDO Disease]
- Left Atrial Pressure [NCIt concept]
- Leucine Aminopeptidase Measurement [NCIt concept]
- Lysosomal Acid Phosphatase [NCIt concept]
- Vocal cord dysfunction familial [MeSH concept]
- acid phosphatase 2, lysosomal [HGNC gene]
- anoperineal lesion [SYNODOS term]
- centromere protein J [ORDO Gene]
- centromere protein J [HGNC gene]
- computerized physician order entry system [MeSH concept]
- leucine aminopeptidase 3 [HGNC gene]
- vocal cord dysfunction familial [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- laryngeal adductor paralysis [MeSH concept]
- laryngeal adductor paralysis [MeSH Supplementary Concept]
False automatic mappings
- PICALM wt Allele [NCIt concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hoarse voice [HPO term]
- Paralysis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital laryngeal adductor palsy (disorder) [SNOMED CT concept]
- laryngeal adductor paralysis [MeSH Supplementary Concept]
- laryngeal adductor paralysis [MeSH concept]

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