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Phakomatosis pigmentokeratotica
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
4 OMIM references -
4 associated genes
No signs/symptoms info
Phakomatosis pigmentokeratotica
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

HRAS
(UniProt - OMIM)
 ARHGDIA
(UniProt - OMIM)
PLCE1
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)
WT1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HRAS
(0.65)
PLCE1


Citations in the biomedical literature:


Phakomatosis pigmentokeratotica
HRAS
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
ARHGDIA PLCE1 PTPRO WT1



Phakomatosis pigmentokeratotica
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: C537893
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.