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1 OMIM reference -
2 associated genes
6 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Dermatofibrosarcoma protuberans
Familial vascular leukoencephalopathy

COL1A1 COL4A1
PDGFB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFB
(0.68)
COL4A1



Citations in the biomedical literature:


Dermatofibrosarcoma protuberans
COL1A1 PDGFB
Familial vascular leukoencephalopathy
COL4A1



Dermatofibrosarcoma protuberans
Familial vascular leukoencephalopathy

Synonym(s):
- DFSP

Synonym(s):
- Brain small vessel disease with hemorrhage
- Retinal arteriolar tortuosity - infantile hemiparesis - autosomal dominant leukoencephalopathy

Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: adult
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C538219
External references:
1 OMIM reference -
1 MeSH reference: C531642

Dermatofibrosarcoma protuberans

Very frequent
- Erythema / erythematous lesions / erythroderma / polymorphous erythema
- Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma)
- Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma
- Subcutaneous nodules / lipomas / tumefaction / swelling
- Thick skin / pachydermia / orange skin

Frequent
- Chronic skin infection / ulcerations / ulcers / cancrum



Familial vascular leukoencephalopathy

(no data available)