Cytoscape Web
Click node...

Ichthyosis prematurity syndrome
1 OMIM reference -
1 associated gene
2 connected diseases
2 signs/symptoms
Disease Type of connection
Congenital non-bullous ichthyosiform erythroderma
Lamellar ichthyosis
Synonym(s):
- Congenital ichthyosis type 4
- IPS
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
(no data available)
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 -
1 MeSH reference: C536271
Gene symbol UniProt reference OMIM reference
SLC27A4 Q6P1M0604194
Very frequent
- Ichthyosis / ichthyosiform dermatitis
- Prematurity