ODCs

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1 associated gene
4 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 1

1 associated gene
11 signs/symptoms

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Cutaneous mastocytoma

KIT

KIT

Citations in the biomedical literature:

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease		Cutaneous mastocytoma
	Synonym(s): (no synonyms)		Synonym(s): - Cutaneous local mastocytoma - Multiple mastocytoma - Solitary mastocytoma

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare allergic disease - Rare hematologic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: sporadic

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

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease		Cutaneous mastocytoma
	Very frequent - Acute leukemia - Eosinophils anomalies / hypereosinophilia - Myeloproliferative syndrome / chronic leukemia		Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Macules - 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