Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the endocrine system (HP:0000818)help
Parent Node:
expandPuberty and gonadal disorders (HP:0008373)help
..Starting node
..expandLeydig cell insensitivity to gonadotropin (HP:0002929)help
Term ID: 2929
Name: Leydig cell insensitivity to gonadotropin
Synonym:
Definition:
Comments:
Reference: HP:0002929
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal circulating estrogen level (HP:0025132) help
..expandAbnormal circulating progesterone level (HP:0031212) help
..expandAbnormal circulating testosterone concentration (HP:0030087) help
..expandAbsence of pubertal development (HP:0008197) help
..expandAbsence of secondary sex characteristics (HP:0008187) help
..expandAdrenogenital syndrome (HP:0000840) help
..expandAndrogen insufficiency (HP:0008226) help
..expandDelayed puberty (HP:0000823) help
..expandEarly onset of sexual maturation (HP:0100000) help
..expandHypogonadism (HP:0000135) help
..expandIrregular menstruation (HP:0000858) help
..expandPrimary gonadal insufficiency (HP:0008193) 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:0002929HP:0002929Leydig cell insensitivity to gonadotropin0ANOS1 CL E G H37306211OMIM:308700Hypogonadotropic hypogonadism 1 with or without anosmia.65


Genes (1) :ANOS1

Diseases (1) :OMIM:308700
 

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