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Acute myelomonocytic leukemia
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
1 OMIM reference -
1 associated gene
3 signs/symptoms
Acute myelomonocytic leukemia
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

FLT3
(UniProt - OMIM)
 APP
(UniProt - OMIM)
NPM1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NPM1
(0.56)
APP


Citations in the biomedical literature:


Acute myelomonocytic leukemia
FLT3 NPM1
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP



Acute myelomonocytic leukemia
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Arctic type
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D015479
External references:
1 OMIM reference -
No MeSH references
Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Acute myelomonocytic leukemia

(no data available)