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Childhood-onset hypophosphatasia
1 OMIM reference -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Adult hypophosphatasia
Infantile hypophosphatasia
Odontohypophosphatasia
Perinatal lethal hypophosphatasia
Prenatal benign hypophosphatasia
Herpetic encephalitis
Huntington disease
Juvenile Huntington disease
Anaplastic ependymoma
Giant cell glioblastoma
Gliosarcoma
Hypohidrotic ectodermal dysplasia with immunodeficiency
Synonym(s):
- Childhood-onset Rathburn disease
- Childhood-onset phosphoethanolaminuria
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ALPL P05186171760
No signs/symptoms info available.