ODCs

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

PROTEIN INTERACTIONS: 2

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

Familial medullary thyroid carcinoma

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

NTRK1	(UniProt - OMIM)		CBL	(UniProt - OMIM)
RET	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RET NTRK1	(0.87) (0.72)	CBL CBL

Citations in the biomedical literature:

Familial medullary thyroid carcinoma		Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
	Synonym(s): - Familial MTC		Synonym(s): - CBL syndrome - Noonan syndrome-like disorder with JMML

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

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

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

	External references: 1 OMIM reference - 1 MeSH reference: C536911		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.