Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormality of movement (HP:0100022)help
..Starting node
..expand
Diminished movement (HP:0002374)help
Term ID: 2374
Name: Diminished movement
Synonym: Diminished movement
Definition:
Comments:
Reference: HP:0002374
Genes and Diseases:
 
       Child Nodes:
........expandAkinesia (HP:0002304) help
........expandHypokinesia (HP:0002375) help

 Sister Nodes: 
..expandAbnormal head movements (HP:0002457) help
..expandAbnormal posturing (HP:0002533) help
..expandAbnormal reflex (HP:0031826) help
..expandAstasia (HP:0020037) help
..expandAsterixis (HP:0012164) help
..expandBimanual synkinesia (HP:0001335) help
..expandCerebral palsy (HP:0100021) help
..expandDyskinesia (HP:0100660) help
..expandDystonia (HP:0001332) help
..expandFrontal release signs (HP:0000743) help
..expandGait disturbance (HP:0001288) help
..expandHyperactivity (HP:0000752) help
..expandHyperkinetic movements (HP:0002487) help
..expandInvoluntary movements (HP:0004305) help
..expandMuscle fibrillation (HP:0010546) help
..expandMyokymia (HP:0002411) help
..expandPostural instability (HP:0002172) help
..expandPrimitive reflex (HP:0002476) help
..expandStooped posture (HP:0025403) 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:0002374HP:0002374Diminished movement0 CL E G H
HP:0002374HP:0002375Hypokinesia1 CL E G H
HP:0002374HP:0002304Akinesia1 CL E G H
HP:0002374HP:0033412Upper extremity akinesia2 CL E G H
HP:0002374HP:0033411Lower extremity akinesia2 CL E G H
HP:0002374HP:0033413Upper extremity hypokinesia2 CL E G H
HP:0002374HP:0033414Lower extremity hypokinesia2 CL E G H


Genes (57) :ACTA1 AIFM1 ATP13A2 CFL2 CHRNA1 CHRND CHRNG CNTN1 DNAJC13 DNAJC6 DOK7 DPM2 EIF4G1 ERBB3 FGF14 FLVCR2 GBA GFM1 GIGYF2 GLRA1 GPHN KLHL40 KLHL41 LAMA2 LAMP2 LMOD3 LRRK2 MAPT MPZ MRPS16 MTM1 MUSK MYOD1 NEB PAM16 PANK2 PDE8B PODXL POLG POLG2 PPP2R2B PRNP RAPSN RRM2B SLC25A4 SLC52A2 SLC6A3 SNCA SYNJ1 TH TMEM240 TPM2 TPM3 TWNK VPS13C VPS35 WWOX

Diseases (40) :171430 171436 171433 238329 300816 606693 253290 612540 411602 391411 994 615042 607598 98764 225790 608013 609060 149400 615348 258 300257 601104 618184 610498 310400 613320 234200 609161 254892 98762 157941 614707 238455 168601 101150 605407 98773 607454 616840 616211
 

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