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1 OMIM reference -
2 associated genes
21 signs/symptoms
COMMON GENES: 1
PROTEIN INTERACTIONS: 5
13 OMIM references -
14 associated genes
No signs/symptoms info
Desmoid tumor
Autosomal dominant nonsyndromic intellectual deficit

APC CACNG2
CTNNB1 CDH15
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


COMMON
GENES
CTNNB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
CTNNB1
APC
CTNNB1
CTNNB1
(0.99)
(0.9)
(0.63)
(0.59)
(0.52)
CTNNB1
TCF4
MBD5
GRIN1
CDH15



Citations in the biomedical literature:


Desmoid tumor
APC CTNNB1
Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4



Desmoid tumor
Autosomal dominant nonsyndromic intellectual deficit

Synonym(s):
- Aggressive fibromatosis
- Desmoid type fibromatosis

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
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 -
No MeSH references
External references:
13 OMIM references -
No MeSH references

Desmoid tumor

Very frequent
- Anomalies of the abdominal wall
- Fibromatosis / bone fibroma
- Muscle anomalies
- Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma
- Subcutaneous nodules / lipomas / tumefaction / swelling

Frequent
- Acute abdominal pain / colic
- Myalgia / muscular pain
- Polyposis of the bowel / colon / intestine

Occasional
- Articular / joint pain / arthralgia
- Bladder and ureter anomalies
- Early death / lethality
- Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia
- Intestinal obstruction / ileus
- Malabsorption / chronic diarrhea / steatorrhea
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Osteolysis / osteoclasia / bone destruction / erosions
- Restricted joint mobility / joint stiffness / ankylosis
- Retinitis pigmentosa / retinal pigmentary changes
- Sepsis severe / septicemia
- Skin tumors / lumps / epidermal cysts
- Thoracic / chest pain


Autosomal dominant nonsyndromic intellectual deficit

(no data available)