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2 OMIM references -
2 associated genes
31 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
22 signs/symptoms
Infantile myofibromatosis
Proteus-like syndrome

NOTCH3 PTEN
PDGFRB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
(0.85)
PTEN



Citations in the biomedical literature:


Infantile myofibromatosis
NOTCH3 PDGFRB
Proteus-like syndrome
PTEN



Infantile myofibromatosis
Proteus-like syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Cohen-Hayden syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease

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

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Irregular / in bands / reticular skin hyperpigmentation


Infantile myofibromatosis
Proteus-like syndrome

Very frequent
- Autosomal dominant inheritance
- Bone cyst
- Bone / osseous neoplasm / tumor / carcinoma / cancer
- Fibromatosis / bone fibroma
- Metaphyseal anomaly
- Muscle anomalies
- Soft tissue sarcoma / cancer / tumor / liposarcoma / myosarcoma
- Subcutaneous nodules / lipomas / tumefaction / swelling

Frequent
- Anomalies of chest / thorax / trunk
- Face / facial anomalies
- Intestinal / colonic anomaly
- Lung / bronchopulmonary neoplasm / tumor / carcinoma / cancer
- Periarticular tissue anomaly / extraarticular calcifications
- Skull / cranial anomalies
- Thickened / hypertrophic / fibromatous gingivae

Occasional
- Anomalies of eyes and vision
- Anomalies of spine, vertebrae and pelvis
- Autosomal recessive inheritance
- Benign tumor of the brain / nervous system
- Chronic skin infection / ulcerations / ulcers / cancrum
- Early death / lethality
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hypercalcemia
- Intestinal obstruction / ileus
- Osteolysis / osteoclasia / bone destruction / erosions
- Pancreatic / pancreas neoplasm / tumor / carcinoma / cancer
- Renal / kidney anomalies
- Restricted joint mobility / joint stiffness / ankylosis
- Sacro-coccyx / sacrum anomaly
- Tracheo-esophageal fistula / esophageal atresia / stenosis


Very frequent
- Asymmetry of the body / hemiatrophy / hemihyperthrophy
- Capillary hemangioma / nevus / naevus flammeus / port-wine stain
- Conjunctival tumor / epibulbar dermoid
- Dental malocclusion
- Exostoses
- Genu recurvatum
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Lower limb asymmetry / hemiatrophy / hemihypertrophy
- Myopia
- Pigmented naevi / naevus pigmentosus / lentigo
- Pupillary anomalies / mydriasis / myosis / tonic pupil
- Xanthomas / lipomas

Frequent
- Cataract / lens opacification
- Communicating hydrocephaly
- Heterochromia / mixed colouring of iris
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Parathyroids anomalies
- Prognathism / prognathia
- Retinal detachment
- Shagreen patch
- Varices / varicous veins / venous insufficiency