Human Phenotype Ontology 
Grandparent Node:
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Abnormal central motor function (HP:0011442)help
Grandparent Node:
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Abnormality of movement (HP:0100022)help
Parent Node:
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Abnormality of extrapyramidal motor function (HP:0002071)help
Parent Node:
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Cerebral palsy (HP:0100021)help
..Starting node
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Athetoid cerebral palsy (HP:0011445)help
Term ID: 11445
Name: Athetoid cerebral palsy
Synonym: Dyskinetic cerebral palsy
Definition: A type of cerebral palsy characterized by slow, involuntary muscle movement and mixed muscle tone.
Comments:
Reference: HP:0011445
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:0011445HP:0011445Athetoid cerebral palsy0CAMK2B CL E G H8161461OMIM:617799Mental retardation, autosomal dominant 54
HP:0011445HP:0011445Athetoid cerebral palsy0RBM10 CL E G H82419896ORPHA:2886TARP syndromeHP:0040284 - Very rare16
HP:0011445HP:0011445Athetoid cerebral palsy0SYT1 CL E G H685711509ORPHA:522077Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndromeHP:0040283 - Occasional1


Genes (3) :CAMK2B RBM10 SYT1

Diseases (3) :OMIM:617799 ORPHA:2886 ORPHA:522077
 

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