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5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
13 signs/symptoms
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cherubism

CEBPA SH3BP2
FLT3
KIT
RUNX1
RUNX1T1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIT
FLT3
(0.72)
(0.63)
SH3BP2
SH3BP2



Citations in the biomedical literature:


Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 KIT RUNX1 RUNX1T1
Cherubism
SH3BP2



Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cherubism

Synonym(s):
(no synonyms)

Synonym(s):
- CRBM

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the digestive system -

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

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D002636

Cherubism

Very frequent
- Autosomal dominant inheritance
- Bone / osseous neoplasm / tumor / carcinoma / cancer
- Enlargment of jaw / large jaw
- High cheek bones

Frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Anodontia / oligodontia / hypodontia
- Tooth shape anomaly

Occasional
- Abnormal cry / voice / phonation disorder / nasal speech
- Apnea / sleep apnea
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Optic nerve anomaly / optic atrophy / anomaly of the papilla
- Proptosis / exophthalmos
- Visual loss / blindness / amblyopia


Acute myeloid leukemia with t(8;21)(q22;q22) translocation

(no data available)