Human Phenotype Ontology 
Grandparent Node:
Abnormal emotion/affect behavior (HP:0100851)help
Parent Node:
Diminished motivation (HP:0000745)help
..Starting node
Akinetic mutism (HP:0012672)help
Term ID: 12672
Name: Akinetic mutism
Definition: Akinetic mutism is essentially characterized by a total absence of spontaneous behavior and speech occurring in the presence of preserved visual tracking.
Reference: HP:0012672
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbulia (HP:0012671) help
..expandApathy (HP:0000741) help
..expandInertia (HP:0030216) 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:0012672HP:0012672Akinetic mutism0DCX CL E G H16412714ORPHA:2148Lissencephaly type 1 due to doublecortin gene mutationHP:0040282 - Frequent145
HP:0012672HP:0012672Akinetic mutism0HTRA1 CL E G H56549476ORPHA:199354Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy34
HP:0012672HP:0012672Akinetic mutism0PRNP CL E G H56219449ORPHA:282166Inherited Creutzfeldt-Jakob diseaseHP:0040282 - Frequent69
HP:0012672HP:0012672Akinetic mutism0SPG21 CL E G H5132420373OMIM:248900Mast syndromeHP:0040283 - Occasional28

Genes (4) :DCX HTRA1 PRNP SPG21

Diseases (4) :ORPHA:2148 ORPHA:199354 ORPHA:282166 OMIM:248900

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