Skip to main content
Diseases

X-Linked Hypophosphatemia

x-linked hypophosphatemia

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
X-Linked Hypophosphatemia
Standard Disease Name
x-linked hypophosphatemia
MeSH Tree
No data
ICD-10
E83.3

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
307800
UMLS ID
C3540852|C3536984|C0733682
HPO ID
No data

Description and Extensions

Description
X-linked hypophosphatemia (XLH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
CYP27B1
cytochrome P450 family 27 subfamily B member 1
cytochrome P450 family 27 subfamily B member 1
02
DMP1
dentin matrix acidic phosphoprotein 1
dentin matrix acidic phosphoprotein 1
04
PHEX
phosphate regulating endopeptidase homolog X-linked
phosphate regulating endopeptidase homolog X-linked
06
SFRP4
secreted frizzled related protein 4
secreted frizzled related protein 4