Peroxisomal Disorders

Disease ID: disease_node_9830

Connections displayed (default: 10).

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Dbxref	ICD10CM:E71.5, ICD9CM:277.86, MESH:D018901, NCI:C85005, SNOMEDCT_US_2023_03_01:238059005, UMLS_CUI:C0282528
Subclassof	DOID_655
Data Source	DOID, MESH
Synonyms	peroxisomal disorder
Mesh Id	D018901
Mesh Label	Peroxisomal Disorders
Mesh Subclassof	D008661
Doid Label	peroxisomal disease
Doid Description	An inherited metabolic disorder that involves peroxisome malfunction.
Disease Node Id	disease_node_9830
Doid Id	DOID_906
Label	Peroxisomal Disorders

Incoming r'ship SUBCLASS_OF to/from Refsum Disease, Infantile(ID:disease_node_11620) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinal Dystrophy With Leukodystrophy(ID:disease_node_17503) (Disease)
Incoming r'ship SUBCLASS_OF to/from Peroxisomal Biogenesis Disorder(ID:disease_node_17504) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mitchell Syndrome(ID:disease_node_17531) (Disease)
Incoming r'ship SUBCLASS_OF to/from Mevalonate Kinase Deficiency(ID:disease_node_11830) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glutaric Acidemia Type 3(ID:disease_node_17501) (Disease)
Incoming r'ship SUBCLASS_OF to/from D-Bifunctional Protein Deficiency(ID:disease_node_17502) (Disease)
Incoming r'ship SUBCLASS_OF to/from Acatalasia(ID:disease_node_10642) (Disease)

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