ODCs

Click node...

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Sebocystomatosis

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT17	(0.63)	CBL

Citations in the biomedical literature:

Sebocystomatosis		Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
	Synonym(s): - Steatocystoma multiplex		Synonym(s): - CBL syndrome - Noonan syndrome-like disorder with JMML

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
(no data available)