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Pilocytic astrocytoma
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Microvillous inclusion disease
1 OMIM reference -
1 associated gene
3 signs/symptoms
Pilocytic astrocytoma
Microvillous inclusion disease

BRAF
(UniProt - OMIM)
 MYO5B
(UniProt - OMIM)
FGFR1
(UniProt - OMIM)
KIAA1549
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NTRK2
(UniProt - OMIM)
RAF1
(UniProt - OMIM)
SRGAP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIAA1549
(0.63)
MYO5B


Citations in the biomedical literature:


Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3
Microvillous inclusion disease
MYO5B



Pilocytic astrocytoma
Microvillous inclusion disease

Synonym(s):
(no synonyms)

Synonym(s):
- Congenital microvillous atrophy
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
Microvillous inclusion disease

Very frequent
- Autosomal recessive inheritance
- Malabsorption / chronic diarrhea / steatorrhea
- Stillbirth / neonatal death



Pilocytic astrocytoma

(no data available)