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Juvenile myelomonocytic leukemia
1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
1 OMIM reference -
1 associated gene
10 signs/symptoms
Juvenile myelomonocytic leukemia
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

CBL
(UniProt - OMIM)
 APP
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NF1
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PTPN11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NF1
KRAS
(0.73)
(0.56)
APP
APP


Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
APP



Juvenile myelomonocytic leukemia
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

Synonym(s):
- Juvenile chronic myelomonocytic leukemia
Synonym(s):
- HCHWA, Iowa 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:
1 OMIM reference -
1 MeSH reference: D054429
External references:
1 OMIM reference -
No MeSH references
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

Very frequent
- Abnormal gait
- Autosomal dominant inheritance
- Cerebral vascular anomalies
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Intracranial / cerebral / meningeal hemorrhage
- Myoclonus / fasciculations
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline
- Transient cerebral ischemia / stroke
- Troubles of memory / amnesia / hypermnesia



Juvenile myelomonocytic leukemia

(no data available)