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Pilocytic astrocytoma

7 associated genes
No signs/symptoms info

COMMON GENES: 1

Osteoglophonic dwarfism

1 OMIM reference -
1 associated gene
20 signs/symptoms

Pilocytic astrocytoma

Osteoglophonic dwarfism

BRAF	(UniProt - OMIM)		FGFR1	(UniProt - OMIM)
FGFR1	(UniProt - OMIM)
KIAA1549	(UniProt - OMIM)
KRAS	(UniProt - OMIM)
NTRK2	(UniProt - OMIM)
RAF1	(UniProt - OMIM)
SRGAP3	(UniProt - OMIM)


COMMON GENES	FGFR1

Citations in the biomedical literature:

Pilocytic astrocytoma		Osteoglophonic dwarfism

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

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

	Epidemiological data: Class of prevalence: - 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 No MeSH references		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
Pilocytic astrocytoma
(no data available)