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Diseases
Hypophosphatemic Rickets, X-Linked Dominant
hypophosphatemic rickets, x-linked dominant
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Hypophosphatemic Rickets, X-Linked Dominant
- Standard Disease Name
- hypophosphatemic rickets, x-linked dominant
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 307800
- UMLS ID
- C0733682|C0733682|C3536984
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An X-linked dominant disorder caused by mutations in the PHEX gene. It is characterized by growth retardation, osteomalacia, hypophosphatemia, and defects in the renal reabsorption of phosphorus.|MSH2017_2016_08_12:An X-linked disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. This disorder is caused by mutations in PHEX PHOSPHATE REGULATING NEUTRAL ENDOPEPTIDASE.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Herbs
target disease -> ingredient target -> herb ingredient8 Herbs
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