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1 associated gene
7 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 1
Bullous diffuse cutaneous mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

KIT KIT


COMMON
GENES
KIT



Citations in the biomedical literature:


Bullous diffuse cutaneous mastocytosis
KIT
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease



Bullous diffuse cutaneous mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Synonym(s):
- Bullous DCM

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references


COMMON
SIGNS
- Mastocytosis


Bullous diffuse cutaneous mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

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

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


Very frequent
- Acute leukemia
- Eosinophils anomalies / hypereosinophilia
- Myeloproliferative syndrome / chronic leukemia