DERMAL RIDGES, NELSON SYNDROME

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 125530
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:0000951) Abnormality of the skin 147 / 7739
2
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
3
 (OMIM) Vertical crack in ridges of hypothenar eminence 2 / 7739
4
 (OMIM) Distal t triradius displacement 2 / 7739
5
 (OMIM) Pointed loop fingertip patterns 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM David (1973) described a family, with the surname Nelson, in which a novel dermatoglyphic syndrome occurred in a mother and 3 of her children. The palmar features were the same as those in ROES (125550), but the only ...