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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
20 signs/symptoms
Craniopharyngioma
Osteoglophonic dwarfism

BRAF FGFR1
CTNNB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.63)
FGFR1



Citations in the biomedical literature:


Craniopharyngioma
BRAF CTNNB1
Osteoglophonic dwarfism
FGFR1



Craniopharyngioma
Osteoglophonic dwarfism

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

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

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
1 MeSH reference: D003397
External references:
1 OMIM reference -
1 MeSH reference: C536050

Osteoglophonic dwarfism

Very frequent
- Abnormal vertebral size / shape
- Anodontia / oligodontia / hypodontia
- Autosomal dominant inheritance
- Craniostenosis / craniosynostosis / sutural synostosis
- Hypertelorism
- Short stature / dwarfism / nanism

Frequent
- Anteverted nares / nostrils
- Clavicle absent / abnormal
- Delayed bone age
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Micrognathia / retrognathia / micrognathism / retrognathism
- Prominent / bat ears
- Rhizomelic micromelia

Occasional
- Abnormal / absent ossification
- Choanal atresia
- Inguinal / inguinoscrotal / crural hernia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Scoliosis
- Short hand / brachydactyly
- Undescended / ectopic testes / cryptorchidia / unfixed testes


Craniopharyngioma

(no data available)