Cytoscape Web
Click node...

Focal palmoplantar keratoderma with joint keratoses
1 OMIM reference -
1 associated gene
22 connected diseases
No signs/symptoms info
Disease Type of connection
Diffuse palmoplantar keratoderma with painful fissures
Keratosis palmoplantaris striata
Severe dermatitis-multiple allergies-metabolic wasting syndrome
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Lethal acantholytic epidermolysis bullosa
Naxos disease
Epidermolysis bullosa simplex due to plakophilin deficiency
Leber congenital amaurosis
Senior-Loken syndrome
Estrogen resistance syndrome
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Isolated growth hormone deficiency type IA
Isolated growth hormone deficiency type IB
Isolated growth hormone deficiency type II
Male infertility with normal virilization due to meiosis defect
Short stature due to growth hormone qualitative anomaly
Spinocerebellar ataxia type 12
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
DSG1 Q02413125670
No signs/symptoms info available.