Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the endocrine system (HP:0000818)help
Parent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormality of the diencephalon (HP:0010662)help
Parent Node:
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Abnormality of the hypothalamus-pituitary axis (HP:0000864)help
..Starting node
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Abnormal hypothalamus physiology (HP:0012285)help
Term ID: 12285
Name: Abnormal hypothalamus physiology
Synonym:
Definition: An abnormal functionality of the hypothalamus.
Comments:
Reference: HP:0012285
Genes and Diseases:
 
       Child Nodes:
........expandHypothalamic gonadotropin-releasing hormone deficiency (HP:0003164) help
........expandHypothalamic hypothyroidism (HP:0008237) help
........expandHypothalamic luteinizing hormone-releasing hormone deficiency (HP:0012287) help

 Sister Nodes: 
..expandAbnormality of the pituitary gland (HP:0012503) 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:0012285HP:0012285Abnormal hypothalamus physiology0 CL E G H
HP:0012285HP:0012287Hypothalamic luteinizing hormone-releasing hormone deficiency1 CL E G H
HP:0012285HP:0008237Hypothalamic hypothyroidism1 CL E G H
HP:0012285HP:0003164Hypothalamic gonadotropin-releasing hormone deficiency1 CL E G H


Genes (24) :ANOS1 CCDC141 CHD7 DCC DUSP6 FEZF1 FGF17 FGF8 FGFR1 FLRT3 HESX1 HS6ST1 IL17RD KISS1R LHX3 NSMF PROK2 PROKR2 SEMA3A SOX10 SPRY4 TACR3 TRH WDR11

Diseases (4) :478 308700 231720 275120
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.