Human Phenotype Ontology 
Grandparent Node:
expand
Limb muscle weakness (HP:0003690)help
Parent Node:
expand
Upper limb muscle weakness (HP:0003484)help
..Starting node
..expand
Wrist drop (HP:0031189)help
Term ID: 31189
Name: Wrist drop
Synonym:
Definition: A condition in which the affected individual cannot extend the wrist, which hangs flaccidly.
Comments:
Reference: HP:0031189
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandProximal muscle weakness in upper limbs (HP:0008997) 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:0031189HP:0031189Wrist drop0ACTA1 CL E G H58129OMIM:616852Myopathy, scapulohumeroperoneal.96
HP:0031189HP:0031189Wrist drop0CADM3 CL E G H5786317601OMIM:619519CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2FF; CMT2FF1
HP:0031189HP:0031189Wrist drop0LDB3 CL E G H1115515710ORPHA:98912Late-onset distal myopathy, Markesbery-Griggs typeHP:0040283 - Occasional286
HP:0031189HP:0031189Wrist drop0MORC2 CL E G H2288023573OMIM:616688Charcot-Marie-Tooth disease, axonal, type 2Z8
HP:0031189HP:0031189Wrist drop0NF2 CL E G H47717773ORPHA:637Neurofibromatosis type 2HP:0040283 - Occasional220
HP:0031189HP:0031189Wrist drop0PLOD1 CL E G H53519081ORPHA:1900Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiencyHP:0040284 - Very rare105
HP:0031189HP:0031189Wrist drop0REEP1 CL E G H6505525786OMIM:62001187


Genes (7) :ACTA1 CADM3 LDB3 MORC2 NF2 PLOD1 REEP1

Diseases (7) :OMIM:616852 OMIM:619519 ORPHA:98912 OMIM:616688 ORPHA:637 ORPHA:1900 OMIM:620011
 

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