ODCs

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1 associated gene
11 signs/symptoms

PROTEIN INTERACTIONS: 2

4 OMIM references -
4 associated genes
No signs/symptoms info

Cutaneous mastocytoma

Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIT KIT	(0.73) (0.52)	PTPRO PLCE1

Citations in the biomedical literature:

Cutaneous mastocytoma		Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
	Synonym(s): - Cutaneous local mastocytoma - Multiple mastocytoma - Solitary mastocytoma		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare allergic disease - Rare hematologic 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: variable Average age of death: normal Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: No OMIM references 1 MeSH reference: D054705		External references: 4 OMIM references - No MeSH references

Cutaneous mastocytoma
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Macules - Mastocytosis - Pruritus / itching - Subcutaneous nodules / lipomas / tumefaction / swelling - Urticaria - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Thick skin / pachydermia / orange skin Occasional - Acute abdominal pain / colic - Facial pain / cephalalgia / migraine - Hot flushes / sensation of cold
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
(no data available)