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:
Adenocarcinoma of the intestines (HP:0040273)

Grandparent Node:
Neoplasm of the small intestine (HP:0100833)

Parent Node:
Adenocarcinoma of the small intestine (HP:0040274)

..Starting node
..Jejunal adenocarcinoma (HP:0030411)

Term ID:

30411

Name:

Jejunal adenocarcinoma

Synonym:

Definition:

A malignant epithelial tumor with a glandular organization that originates in the jejunum.

Comments:

Reference:

HP:0030411

Genes and Diseases:

Child Nodes:

Sister Nodes:

Duodenal adenocarcinoma (HP:0006771)

Ileal adenocarcinoma (HP:0030412)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030411	HP:0030411	Jejunal adenocarcinoma	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.