Human Phenotype Ontology 
Grandparent Node:
expandAbnormal morphology of the abdominal musculature (HP:0010991)help
Grandparent Node:
expandMuscle weakness (HP:0001324)help
Parent Node:
expandAbdominal wall muscle weakness (HP:0009023)help
..Starting node
..expandBeevor's sign (HP:0030664)help
Term ID: 30664
Name: Beevor's sign
Synonym:
Definition: Weakness of the inferior portion of the rectus abdominal muscle, which is ascertained clinically as follows. When a patient sits up or raises the head from a recumbent position, the umbilicus is displaced toward the head. This is the result of paralysis of the inferior portion of the rectus abdominal muscle, so that the upper fibres predominate pulling upwards the umbilicus.
Comments:
Reference: HP:0030664
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030664HP:0030664Beevor's sign0FRG1 CL E G H24833954OMIM:158900Facioscapulohumeral muscular dystrophy 1.1
HP:0030664HP:0030664Beevor's sign0MYH7 CL E G H46257577ORPHA:437572MYH7-related late-onset scapuloperoneal muscular dystrophyHP:0040283 - Occasional1269
HP:0030664HP:0030664Beevor's sign0SMCHD1 CL E G H2334729090OMIM:158901FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2174


Genes (3) :FRG1 MYH7 SMCHD1

Diseases (3) :OMIM:158900 ORPHA:437572 OMIM:158901
 

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