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3 associated genes
No signs/symptoms info
COMMON GENES: 1
1 associated gene
11 signs/symptoms
Acute myeloblastic leukemia with maturation
Cutaneous mastocytoma

FLT3 KIT
KIT
NPM1


COMMON
GENES
KIT



Citations in the biomedical literature:


Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1
Cutaneous mastocytoma



Acute myeloblastic leukemia with maturation
Cutaneous mastocytoma

Synonym(s):
- Acute myeloblastic leukemia type 2

Synonym(s):
- Cutaneous local mastocytoma
- Multiple mastocytoma
- Solitary mastocytoma

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: unknown
Average age onset: variable
Average age of death: normal
Type of inheritance: sporadic

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: D054705

Cutaneous mastocytoma

Very frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Macules
- Mastocytosis
- Pruritus / itching
- Subcutaneous nodules / lipomas / tumefaction / swelling
- Urticaria
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Frequent
- Thick skin / pachydermia / orange skin

Occasional
- Acute abdominal pain / colic
- Facial pain / cephalalgia / migraine
- Hot flushes / sensation of cold


Acute myeloblastic leukemia with maturation

(no data available)