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Diseases

Albright's hereditary osteodystrophy

albright's hereditary osteodystrophy

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Albright's hereditary osteodystrophy
Standard Disease Name
albright's hereditary osteodystrophy
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D020257
OMIM ID
No data
UMLS ID
C0600519
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12:The geometric and structural changes that the HEART VENTRICLES undergo, usually following MYOCARDIAL INFARCTION. It comprises expansion of the infarct and dilatation of the healthy ventricle segments. While most prevalent in the left ventricle, it can also occur in the right ventricle.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
01
ASAH1
N-acylsphingosine amidohydrolase 1
N-acylsphingosine amidohydrolase 1
02
CFTR
CF transmembrane conductance regulator
CF transmembrane conductance regulator
07
PRKAR1A
protein kinase cAMP-dependent type I regulatory subunit alpha
protein kinase cAMP-dependent type I regulatory subunit alpha