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
..Viral infection-induced rhabdomyolysis (HP:0003558)

Term ID:

3558

Name:

Viral infection-induced rhabdomyolysis

Synonym:

Definition:

Rhabdomyolysis induced by a viral infection.

Comments:

Reference:

HP:0003558

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acute rhabdomyolysis (HP:0008942)

Alcohol-induced rhabdomyolysis (HP:0011440)

Anesthetic-induced rhabdomylosis (HP:0011439)

Exercise-induced rhabdomyolysis (HP:0009045)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	ALDOA CL E G H	226	414	ORPHA:57	Glycogen storage disease due to aldolase A deficiency	HP:0040282 - Frequent	50
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	COX1 CL E G H	4512	7419	ORPHA:99845	Genetic recurrent myoglobinuria
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	COX3 CL E G H	4514	7422	ORPHA:99845	Genetic recurrent myoglobinuria
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	DGUOK CL E G H	1716	2858	ORPHA:329314	Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency	HP:0040283 - Occasional	57
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	LPIN1 CL E G H	23175	13345	ORPHA:99845	Genetic recurrent myoglobinuria		95
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	SEPSECS CL E G H	51091	30605	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040283 - Occasional	66
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	TSEN15 CL E G H	116461	16791	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040283 - Occasional	3
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	TSEN2 CL E G H	80746	28422	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040283 - Occasional	84
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	TSEN34 CL E G H	79042	15506	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040283 - Occasional	57
HP:0003558	HP:0003558	Viral infection-induced rhabdomyolysis	0	TSEN54 CL E G H	283989	27561	ORPHA:2524	Pontocerebellar hypoplasia type 2	HP:0040283 - Occasional	102

Genes (10) :ALDOA COX1 COX3 DGUOK LPIN1 SEPSECS TSEN15 TSEN2 TSEN34 TSEN54

Diseases (4) :ORPHA:57 ORPHA:99845 ORPHA:329314 ORPHA:2524

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

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