Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
2 OMIM references -
3 associated genes
12 signs/symptoms
Papilloma of choroid plexus
Isolated brachycephaly

TP53 FGFR3
TCF12
TWIST1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TP53
(0.88)
TWIST1



Citations in the biomedical literature:


Papilloma of choroid plexus
TP53
Isolated brachycephaly
FGFR3 TCF12 TWIST1



Papilloma of choroid plexus
Isolated brachycephaly

Synonym(s):
(no synonyms)

Synonym(s):
- Non-syndromic bicornal synostosis

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D020288
External references:
2 OMIM references -
No MeSH references


COMMON
SIGNS
- Intellectual deficit / mental / psychomotor retardation / learning disability


Papilloma of choroid plexus
Isolated brachycephaly

Very frequent
- Autosomal recessive inheritance
- Central nervous system / peripheral nerves neoplasm / tumor / carcinoma / cancer
- Hydrocephaly
- Structural anomalies of the nervous system

Occasional
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hypertonia / spasticity / rigidity / stiffness
- Mild visual loss / impaired visual acuity
- Neoplasms / tumors
- Seizures / epilepsy / absences / spasms / status epilepticus


Very frequent
- Brachycephaly / flat occiput
- Broad forehead

Frequent
- Cranial hypertension
- Flat supraorbital ridge
- Hearing loss / hypoacusia / deafness
- Proptosis / exophthalmos

Occasional
- Autosomal dominant inheritance
- Hypertelorism
- Metacarpal anomalies / Archibald's sign
- Mid-facial hypoplasia / short / small midface
- Short hand / brachydactyly