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Autosomal recessive hypophosphatemic rickets
2 OMIM references -
2 associated genes
12 connected diseases
No signs/symptoms info
Disease Type of connection
Generalized arterial calcification of infancy
Hypopigmentation-punctate palmoplantar keratoderma syndrome
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Rabson-Mendenhall syndrome
Amyotrophic lateral sclerosis
Atypical hemolytic uremic syndrome with H factor anomaly
Dense deposit disease
Familial drusen
Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Synonym(s):
- ARHR
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
DMP1 Q13316600980
ENPP1 P22413173335
No signs/symptoms info available.