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 breast morphology (HP:0031093)

Grandparent Node:
Neoplasm by anatomical site (HP:0011793)

Parent Node:
Neoplasm of the breast (HP:0100013)

..Starting node
..Lobular carcinoma in situ (HP:0030076)

Term ID:

30076

Name:

Lobular carcinoma in situ

Synonym:

Definition:

Comments:

Reference:

HP:0030076

Genes and Diseases:

Child Nodes:

Sister Nodes:

Breast carcinoma (HP:0003002)

Ductal carcinoma in situ (HP:0030075)

Fibroadenoma of the breast (HP:0010619)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030076	HP:0030076	Lobular carcinoma in situ	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.