Human Phenotype Ontology 
Grandparent Node:
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Abnormal autonomic nervous system physiology (HP:0012332)help
Parent Node:
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obsolete Dysautonomia (HP:0002459)help
..Starting node
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Autonomic erectile dysfunction (HP:0008652)help
Term ID: 8652
Name: Autonomic erectile dysfunction
Synonym: Impotence due to autonomic dysfunction
Definition: Impotence (inability to develop or maintain an erection) resulting from abnormal functioning of the autonomic nervous system.
Comments:
Reference: HP:0008652
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAutonomic bladder dysfunction (HP:0005341) 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:0008652HP:0008652Autonomic erectile dysfunction0COQ2 CL E G H2723525223ORPHA:227510Multiple system atrophy, cerebellar typeHP:0040282 - Frequent54
HP:0008652HP:0008652Autonomic erectile dysfunction0COQ2 CL E G H2723525223ORPHA:98933Multiple system atrophy, parkinsonian typeHP:0040282 - Frequent54
HP:0008652HP:0008652Autonomic erectile dysfunction0LMNB1 CL E G H40016637OMIM:169500Leukodystrophy, adult-onset, autosomal dominant44


Genes (2) :COQ2 LMNB1

Diseases (3) :ORPHA:227510 ORPHA:98933 OMIM:169500
 

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