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Prenatal benign hypophosphatasia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Anaplastic ependymoma
2 associated genes
No signs/symptoms info
Prenatal benign hypophosphatasia
Anaplastic ependymoma

ALPL
(UniProt - OMIM)
 C11ORF95
(UniProt - OMIM)
RELA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ALPL
(0.49)
RELA


Citations in the biomedical literature:


Prenatal benign hypophosphatasia
ALPL
Anaplastic ependymoma
C11ORF95 RELA



Prenatal benign hypophosphatasia
Anaplastic ependymoma

Synonym(s):
- Prenatal benign Rathburn disease
- Prenatal benign phosphoethanolaminuria
Synonym(s):
- High-grade ependymoma
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.