Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal skeletal muscle morphology (HP:0011805)

Parent Node:
Rhabdomyolysis (HP:0003201)

..Starting node
..Alcohol-induced rhabdomyolysis (HP:0011440)

Term ID:

11440

Name:

Alcohol-induced rhabdomyolysis

Synonym:

Definition:

Rhabdomyolysis induced by intake of alcohol.

Comments:

Reference:

HP:0011440

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acute rhabdomyolysis (HP:0008942)

Anesthetic-induced rhabdomylosis (HP:0011439)

Exercise-induced rhabdomyolysis (HP:0009045)

Viral infection-induced rhabdomyolysis (HP:0003558)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011440	HP:0011440	Alcohol-induced rhabdomyolysis	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.