Cytoscape Web
Click node...


1 OMIM reference -
2 associated genes
11 signs/symptoms
COMMON GENES: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Isolated plagiocephaly
Extraskeletal myxoid chondrosarcoma

FGFR3 EWSR1
TCF12 NR4A3
TAF15
TCF12
TFG


COMMON
GENES
TCF12



Citations in the biomedical literature:


Isolated plagiocephaly
FGFR3 TCF12
Extraskeletal myxoid chondrosarcoma
EWSR1 NR4A3 TAF15 TFG



Isolated plagiocephaly
Extraskeletal myxoid chondrosarcoma

Synonym(s):
- Non-syndromic unicoronal synostosis
- Synostotic plagiocephaly

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic

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

Isolated plagiocephaly

Very frequent
- Facial structural asymmetry / facial hemiatrophy / facial hemihypertrophy
- Frontal bossing / prominent forehead
- Plagiocephaly

Frequent
- Abnormal eye movements / oculomotor disorder
- Abnormal visual field / hemianopsia / hemianopia / scotoma / visual peripheral rim
- Strabismus / squint

Occasional
- Autosomal dominant inheritance
- Hearing loss / hypoacusia / deafness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Mid-facial hypoplasia / short / small midface


Extraskeletal myxoid chondrosarcoma

(no data available)