Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the breast (HP:0000769)help
Parent Node:
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Abnormal breast physiology (HP:0031094)help
..Starting node
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Galactorrhea (HP:0100829)help
Term ID: 100829
Name: Galactorrhea
Synonym: Galactorrhoea; Spontaneous milk flow from breast
Definition: Spontaneous flow of milk from the breast, unassociated with childbirth or nursing.
Comments:
Reference: HP:0100829
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgalactia (HP:0031109) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100829HP:0100829Galactorrhea0AIP CL E G H9049358ORPHA:963AcromegalyHP:0040283 - Occasional95
HP:0100829HP:0100829Galactorrhea0AIP CL E G H9049358OMIM:102200Pituitary adenoma, growth hormone-secreting, 1.95
HP:0100829HP:0100829Galactorrhea0AIP CL E G H9049358ORPHA:99725Pituitary gigantismHP:0040283 - Occasional95
HP:0100829HP:0100829Galactorrhea0AIP CL E G H9049358ORPHA:2965ProlactinomaHP:0040281 - Very frequent95
HP:0100829HP:0100829Galactorrhea0CDH23 CL E G H6407213733ORPHA:2965ProlactinomaHP:0040281 - Very frequent636
HP:0100829HP:0100829Galactorrhea0CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040282 - Frequent2
HP:0100829HP:0100829Galactorrhea0CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040282 - Frequent102
HP:0100829HP:0100829Galactorrhea0CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040282 - Frequent1
HP:0100829HP:0100829Galactorrhea0CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040282 - Frequent
HP:0100829HP:0100829Galactorrhea0GPR101 CL E G H8355014963ORPHA:963AcromegalyHP:0040283 - Occasional5
HP:0100829HP:0100829Galactorrhea0IRF4 CL E G H36626119ORPHA:3452Whipple diseaseHP:0040283 - Occasional1
HP:0100829HP:0100829Galactorrhea0MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040282 - Frequent462
HP:0100829HP:0100829Galactorrhea0MEN1 CL E G H42217010ORPHA:99725Pituitary gigantismHP:0040283 - Occasional462
HP:0100829HP:0100829Galactorrhea0MEN1 CL E G H42217010ORPHA:2965ProlactinomaHP:0040281 - Very frequent462
HP:0100829HP:0100829Galactorrhea0PRLR CL E G H56189446ORPHA:397685Familial hyperprolactinemiaHP:0040281 - Very frequent2
HP:0100829HP:0100829Galactorrhea0PRLR CL E G H56189446OMIM:615555HYPERPROLACTINEMIAHP:0040283 - Occasional2


Genes (10) :AIP CDH23 CDKN1A CDKN1B CDKN2B CDKN2C GPR101 IRF4 MEN1 PRLR

Diseases (8) :ORPHA:963 OMIM:102200 ORPHA:99725 ORPHA:2965 ORPHA:652 ORPHA:3452 ORPHA:397685 OMIM:615555
 

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