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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 associated gene
7 signs/symptoms
Juvenile myelomonocytic leukemia
Bullous diffuse cutaneous mastocytosis

CBL KIT
KRAS
NF1
NRAS
PTPN11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN11
CBL
(0.9)
(0.75)
KIT
KIT



Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Bullous diffuse cutaneous mastocytosis
KIT



Juvenile myelomonocytic leukemia
Bullous diffuse cutaneous mastocytosis

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

Synonym(s):
- Bullous DCM

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare allergic disease
- Rare hematologic disease
- Rare oncologic disease
- Rare skin disease

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
1 MeSH reference: D054429
External references:
No OMIM references
No MeSH references

Bullous diffuse cutaneous mastocytosis

Very frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Mastocytosis
- Pruritus / itching
- Urticaria
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Occasional
- Collapse / sudden death / cardiac arrest / cardiorespiratory arrest


Juvenile myelomonocytic leukemia

(no data available)