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1 OMIM reference -
2 associated genes
6 signs/symptoms
COMMON GENES: 1
PROTEIN INTERACTIONS: 2
1 OMIM reference -
3 associated genes
29 signs/symptoms
Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1

COL1A1 COL1A1
PDGFB COL5A1
COL5A2


COMMON
GENES
COL1A1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFB
PDGFB
(0.81)
(0.68)
COL1A1
COL5A1



Citations in the biomedical literature:


Dermatofibrosarcoma protuberans
COL1A1 PDGFB
Ehlers-Danlos syndrome type 1
COL5A1 COL5A2



Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1

Synonym(s):
- DFSP

Synonym(s):
- EDS I

Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
- Rare skin disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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: 1-9 / 100 000
Average age onset: neonatal/infancy
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: C536194

Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1

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



Very frequent
- Autosomal dominant inheritance
- Hyperextensible joints / articular hyperlaxity
- Joint dislocation / subluxation
- Skin hypoplasia / aplasia / atrophy
- Thin skin

Frequent
- Aortic dilatation / dilation
- Bruisability
- Diaphragmatic hernia / defect / agenesis
- Flat foot
- Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia
- Genu recurvatum
- Hallux valgus
- Herniae
- Inguinal / inguinoscrotal / crural hernia
- Pectus carinatum
- Pectus excavatum
- Scoliosis
- Umbilical hernia
- Varices / varicous veins / venous insufficiency

Occasional
- Aortic dissection
- Bladder / vesical diverticulum
- Cardiac valvulopathy
- Chronic arterial hypertension
- Mitral valve prolapse / incompetence / insufficiency / regurgitation / ring anomaly
- Oral synechiae / abnormal frenulae
- Peritonitis / peritoneal abscess
- Recurrent urinary infections
- Retinal detachment
- Skin tumors / lumps / epidermal cysts