LARYNGEAL ADDUCTOR PARALYSIS

General Information (adopted from Orphanet):

Synonyms, Signs: VOCAL CORD DYSFUNCTION, ADDUCTOR TYPE
LAP
Number of Symptoms 4
OrphanetNr:
OMIM Id: 150270
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0001609) Hoarse voice 34 / 7739
2
 (OMIM) Congential hoarseness 1 / 7739
3
 (OMIM) Laryngeal adductor paralysis 1 / 7739
4
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Mace et al. (1978) described a family with congenital bilateral adductor paralysis in 10 persons in 5 generations. Hoarseness from birth with some progression was the only symptom.

Also see abductor laryngeal paralysis (150260 and 308850). ...