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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Hypophosphatemic Rickets, X-Linked Dominant

hypophosphatemic rickets, x-linked dominant

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Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

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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.