Human Phenotype Ontology

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:
Abnormality of the breast (HP:0000769)

Parent Node:
Abnormal breast physiology (HP:0031094)

..Starting node
..Agalactia (HP:0031109)

Term ID:

31109

Name:

Agalactia

Synonym:

Lactation incapacity

Definition:

Failure of secretion of milk following childbirth associated with an inability to breastfeed an infant.

Comments:

Reference:

HP:0031109

Genes and Diseases:

Child Nodes:

Sister Nodes:

Galactorrhea (HP:0100829)

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:0031109	HP:0031109	Agalactia	0	PRLR CL E G H	5618	9446	OMIM:615555	HYPERPROLACTINEMIA	HP:0040284 - Very rare	2

Genes (1) :PRLR

Diseases (1) :OMIM:615555

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