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Diseases

Farber Disease

farber disease

Entity Type
Diseases
Relation Groups
3
Relation Preview
23

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
Farber Disease
Standard Disease Name
farber disease
MeSH Tree
No data
ICD-10
E75.2

Identifiers

DO ID
No data
MeSH ID
D055577|C537075
OMIM ID
228000
UMLS ID
C2936785|C0268255
HPO ID
No data

Description and Extensions

Description
Farber disease is a rare sphingolipid disorder characterized by a spectrum of clinical signs ranging from the classical triad of painful and progressively deformed joints, subcutaneous nodules, and pr
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease7 Targets
02
ASAH1
N-acylsphingosine amidohydrolase 1
N-acylsphingosine amidohydrolase 1
05
NAGA
alpha-N-acetylgalactosaminidase
alpha-N-acetylgalactosaminidase