KERATOSIS, FAMILIAL ACTINIC

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 148390
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:0010784) Uterine neoplasm 13 / 7739
2
 (HPO:0000951) Abnormality of the skin 147 / 7739
3
 (HPO:0001939) Abnormality of metabolism/homeostasis 328 / 7739
4
 (HPO:0002664) Neoplasm 111 / 7739
5
 (OMIM) Cutaneous pigmented actinic keratoses 1 / 7739
6
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
7
 (OMIM) Fibroblasts show gross cytopathic changes, low survival indices, and increased DNA single-strand break frequency following long-wave ultraviolet radiation exposure 1 / 7739
8
 (OMIM) Uterine carcinoma 1 / 7739
9
 (OMIM) Internal malignancies 2 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: