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:
Glandular cell neoplasm (HP:0031493)

Parent Node:
Mucinous neoplasm (HP:0031495)

..Starting node
..Mucinous cystic neoplasm of the pancreas (HP:0031496)

Term ID:

31496

Name:

Mucinous cystic neoplasm of the pancreas

Synonym:

Definition:

Mucin-producing and septated cyst-forming epithelial neoplasia of the pancreas with a distinctive ovarian-type stroma.

Comments:

Reference:

HP:0031496

Genes and Diseases:

Child Nodes:

Sister Nodes:

Appendiceal mucinous neoplasm (HP:0031499)

Mucinous colorectal carcinoma (HP:0031497)

Mucinous gastric carcinoma (HP:0031498)

Ovarian mucinous tumor (HP:0031494)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031496	HP:0031496	Mucinous cystic neoplasm of the pancreas	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.