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1 OMIM reference -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Chronic myeloid leukemia
Familial medullary thyroid carcinoma

ABL1 NTRK1
BCR RET
RUNX1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ABL1
(0.89)
NTRK1



Citations in the biomedical literature:


Chronic myeloid leukemia
ABL1 BCR RUNX1
Familial medullary thyroid carcinoma
NTRK1 RET



Chronic myeloid leukemia
Familial medullary thyroid carcinoma

Synonym(s):
- Chronic granulocytic leukemia
- Chronic myelogenous leukemia

Synonym(s):
- Familial MTC

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.