Human Phenotype Ontology 
Grandparent Node:
Abnormality of the endocrine system (HP:0000818)help
Parent Node:
Abnormal nervous system physiology (HP:0012638)help
Parent Node:
Abnormality of the pineal gland (HP:0012680)help
..Starting node
Abnormality of pineal physiology (HP:0012688)help
Term ID: 12688
Name: Abnormality of pineal physiology
Definition: A functional abnormality of the pineal gland.
Reference: HP:0012688
Genes and Diseases:
       Child Nodes:
........expandAbnormal pineal melatonin secretion (HP:0012689) help

 Sister Nodes: 
..expandAbnormal pineal morphology (HP:0012681) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012688HP:0012688Abnormality of pineal physiology0 CL E G H
HP:0012688HP:0012689Abnormal pineal melatonin secretion1 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 August 2021 release.