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Sebocystomatosis

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Myelofibrosis with myeloid metaplasia

1 OMIM reference -
4 associated genes
No signs/symptoms info

Sebocystomatosis

Myelofibrosis with myeloid metaplasia

KRT17	(UniProt - OMIM)		CALR	(UniProt - OMIM)
			JAK2	(UniProt - OMIM)
			MPL	(UniProt - OMIM)
			TET2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT17	(0.49)	CALR

Citations in the biomedical literature:

Sebocystomatosis		Myelofibrosis with myeloid metaplasia
	Synonym(s): - Steatocystoma multiplex		Synonym(s): - Agnogenic myeloid metaplasia - Idiopathic myelofibrosis - Myelosclerosis with myeloid metaplasia - Primary myelofibrosis

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

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

Sebocystomatosis
	Very frequent - Adenoma sebaceum - Autosomal dominant inheritance - Skin tumors / lumps / epidermal cysts Occasional - Urinary / renal lithiasis / kidney stones / nephritic colic
Myelofibrosis with myeloid metaplasia
(no data available)