POLYDACTYLY, POSTAXIAL, TYPE A2

General Information (adopted from Orphanet):

Synonyms, Signs: POSTAXIAL POLYDACTYLY, TYPE A2
PAPA2
Number of Symptoms 3
OrphanetNr:
OMIM Id: 602085
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:0001162) Postaxial hand polydactyly 119 / 7739
2
(HPO:0100259) Postaxial polydactyly 85 / 7739
3
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Van der Zwaag et al. (2010) studied a 27-month-old boy who was born with bilateral postaxial polydactyly of the hands. The extra sixth digits, which were removed surgically, consisted of soft tissue only, although a nail was present ...