Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal central motor function (HP:0011442)help
Parent Node:
expand
Rigidity (HP:0002063)help
..Starting node
..expand
Decerebrate rigidity (HP:0025013)help
Term ID: 25013
Name: Decerebrate rigidity
Synonym: Decerebrate posturing
Definition: A type of rigidity that is manifested by an exaggerated extensor posture of all extremities.
Comments:
Reference: HP:0025013
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCogwheel rigidity (HP:0002396) help
..expandDecorticate rigidity (HP:0011444) help
..expandExtrapyramidal muscular rigidity (HP:0007076) 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:0025013HP:0025013Decerebrate rigidity0ARSA CL E G H410713ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare253
HP:0025013HP:0025013Decerebrate rigidity0ARSA CL E G H410713ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040284 - Very rare253
HP:0025013HP:0025013Decerebrate rigidity0ARSA CL E G H410713ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040284 - Very rare253
HP:0025013HP:0025013Decerebrate rigidity0ASPA CL E G H443756ORPHA:314911Severe Canavan diseaseHP:0040284 - Very rare48
HP:0025013HP:0025013Decerebrate rigidity0GALC CL E G H25814115ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional160
HP:0025013HP:0025013Decerebrate rigidity0GALC CL E G H25814115OMIM:245200Krabbe disease.160
HP:0025013HP:0025013Decerebrate rigidity0GLB1 CL E G H27204298ORPHA:79255GM1 gangliosidosis type 1HP:0040283 - Occasional120
HP:0025013HP:0025013Decerebrate rigidity0PSAP CL E G H56609498ORPHA:206436Infantile Krabbe diseaseHP:0040283 - Occasional81
HP:0025013HP:0025013Decerebrate rigidity0PSAP CL E G H56609498ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare81
HP:0025013HP:0025013Decerebrate rigidity0PSAP CL E G H56609498ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040284 - Very rare81
HP:0025013HP:0025013Decerebrate rigidity0PSAP CL E G H56609498ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040284 - Very rare81


Genes (5) :ARSA ASPA GALC GLB1 PSAP

Diseases (7) :ORPHA:309271 ORPHA:309263 ORPHA:309256 ORPHA:314911 ORPHA:206436 OMIM:245200 ORPHA:79255
 

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