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

ARHGDIA MEFV
PLCE1 TNFRSF1A
PTPRO
WT1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ARHGDIA
(0.55)
TNFRSF1A



Citations in the biomedical literature:


Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
ARHGDIA PLCE1 PTPRO WT1
Intermittent hydrarthrosis
MEFV TNFRSF1A



Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Intermittent hydrarthrosis

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
4 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.