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Bathing suit ichthyosis
1 OMIM reference -
1 associated gene
8 connected diseases
2 signs/symptoms
Disease Type of connection
Congenital non-bullous ichthyosiform erythroderma
Self-healing collodion baby
Lamellar ichthyosis
Acral self-healing collodion baby
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Parkinsonian-pyramidal syndrome
Young adult-onset Parkinsonism
Synonym(s):
- BSI
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
TGM1 P22735190195
Very frequent
- Autosomal recessive inheritance
- Ichthyosis / ichthyosiform dermatitis