Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

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:
Constitutional symptom (HP:0025142)

Parent Node:
Pain (HP:0012531)

..Starting node
..Epigastric pain (HP:0410019)

Term ID:

410019

Name:

Epigastric pain

Synonym:

Epigastrium pain

Definition:

Pain that is localized to the region of the upper abdomen immediately below the ribs.

Comments:

Reference:

HP:0410019

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abdominal pain (HP:0002027)

Allodynia (HP:0012533)

Anal pain (HP:0500005)

Ankle pain (HP:0030840)

Arthralgia (HP:0002829)

Back pain (HP:0003418)

Bone pain (HP:0002653)

Chest pain (HP:0100749)

Chronic pain (HP:0012532)

Costochondral pain (HP:0006649)

Ear pain (HP:0030766)

Elbow pain (HP:0030835)

Finger pain (HP:0030837)

Flank pain (HP:0030157)

Foot pain (HP:0025238)

Groin pain (HP:0031520)

Hip pain (HP:0030838)

Jaw pain (HP:0040264)

Knee pain (HP:0030839)

Limb pain (HP:0009763)

Mandibular pain (HP:0200025)

Myalgia (HP:0003326)

Neck pain (HP:0030833)

Ocular pain (HP:0200026)

Scrotal pain (HP:0030155)

Shoulder pain (HP:0030834)

Toe pain (HP:0030841)

Vulvodynia (HP:0030943)

Wrist pain (HP:0030836)

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:0410019	HP:0410019	Epigastric pain	0	ALMS1 CL E G H	7840	428	ORPHA:64	Alström syndrome	HP:0040283 - Occasional	404
HP:0410019	HP:0410019	Epigastric pain	0	CD46 CL E G H	4179	6953	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	39
HP:0410019	HP:0410019	Epigastric pain	0	CFH CL E G H	3075	4883	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	86
HP:0410019	HP:0410019	Epigastric pain	0	CFI CL E G H	3426	5394	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	57
HP:0410019	HP:0410019	Epigastric pain	0	CTNNB1 CL E G H	1499	2514	ORPHA:33402	Pediatric hepatocellular carcinoma	HP:0040282 - Frequent	88
HP:0410019	HP:0410019	Epigastric pain	0	CTRC CL E G H	11330	2523	ORPHA:103918	Tropical pancreatitis		39
HP:0410019	HP:0410019	Epigastric pain	0	HELLPAR CL E G H	101101692	43984	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional
HP:0410019	HP:0410019	Epigastric pain	0	MET CL E G H	4233	7029	ORPHA:33402	Pediatric hepatocellular carcinoma	HP:0040282 - Frequent	375
HP:0410019	HP:0410019	Epigastric pain	0	SPINK1 CL E G H	6690	11244	ORPHA:103918	Tropical pancreatitis		34

Genes (9) :ALMS1 CD46 CFH CFI CTNNB1 CTRC HELLPAR MET SPINK1

Diseases (4) :ORPHA:64 ORPHA:244242 ORPHA:33402 ORPHA:103918

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

Feedback about the webpages , or email to MSeqDR webmaster: Lishuang Shen