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 blood glucose concentration (HP:0011015)

Parent Node:
Hyperglycemia (HP:0003074)

..Starting node
..Postprandial hyperglycemia (HP:0011998)

Term ID:

11998

Name:

Postprandial hyperglycemia

Synonym:

Definition:

An increased concentration of glucose in the blood following a meal.

Comments:

Reference:

HP:0011998

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0011998	HP:0011998	Postprandial hyperglycemia	0	CACNA1S CL E G H	779	1397	ORPHA:681	Hypokalemic periodic paralysis	HP:0040282 - Frequent	247
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	CACNA1S CL E G H	779	1397	ORPHA:79102	Thyrotoxic periodic paralysis	HP:0040282 - Frequent	247
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	GABRA3 CL E G H	2556	4077	ORPHA:79102	Thyrotoxic periodic paralysis	HP:0040282 - Frequent
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	GYS2 CL E G H	2998	4707	OMIM:240600	Glycogen storage disease 0, liver	.	100
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	GYS2 CL E G H	2998	4707	ORPHA:2089	Glycogen storage disease due to hepatic glycogen synthase deficiency	HP:0040282 - Frequent	100
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	INSR CL E G H	3643	6091	OMIM:246200	Donohue syndrome	.	229
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	INSR CL E G H	3643	6091	ORPHA:508	Leprechaunism	HP:0040281 - Very frequent	229
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	INSR CL E G H	3643	6091	OMIM:262190	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities	.	229
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	INSR CL E G H	3643	6091	ORPHA:769	Rabson-Mendenhall syndrome	HP:0040282 - Frequent	229
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	KCNE3 CL E G H	10008	6243	ORPHA:681	Hypokalemic periodic paralysis	HP:0040282 - Frequent	73
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	KCNJ18 CL E G H	100134444	39080	ORPHA:79102	Thyrotoxic periodic paralysis	HP:0040282 - Frequent	10
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	SCN4A CL E G H	6329	10591	ORPHA:681	Hypokalemic periodic paralysis	HP:0040282 - Frequent	263
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	SHPK CL E G H	23729	1492	ORPHA:440713	Isolated sedoheptulokinase deficiency	HP:0040282 - Frequent	2
HP:0011998	HP:0011998	Postprandial hyperglycemia	0	SLC2A2 CL E G H	6514	11006	ORPHA:2088	Fanconi-Bickel syndrome	HP:0040282 - Frequent	71

Genes (9) :CACNA1S GABRA3 GYS2 INSR KCNE3 KCNJ18 SCN4A SHPK SLC2A2

Diseases (10) :ORPHA:681 ORPHA:79102 OMIM:240600 ORPHA:2089 OMIM:246200 ORPHA:508 OMIM:262190 ORPHA:769 ORPHA:440713 ORPHA:2088

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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