Human Phenotype Ontology 
Grandparent Node:
Abnormal nervous system physiology (HP:0012638)help
Parent Node:
Abnormality of movement (HP:0100022)help
..Starting node
Asterixis (HP:0012164)help
Term ID: 12164
Name: Asterixis
Definition: A clinical sign indicating a lapse of posture and is usually manifest by a bilateral flapping tremor at the wrist, metacarpophalangeal, and hip joints.
Reference: HP:0012164
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal head movements (HP:0002457) help
..expandAbnormal posturing (HP:0002533) help
..expandAbnormal reflex (HP:0031826) help
..expandAstasia (HP:0020037) help
..expandBimanual synkinesia (HP:0001335) help
..expandCerebral palsy (HP:0100021) help
..expandDiminished movement (HP:0002374) 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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012164HP:0012164Asterixis0ABCB11 CL E G H864742ORPHA:69665Intrahepatic cholestasis of pregnancyHP:0040284 - Very rare146
HP:0012164HP:0012164Asterixis0ABCB4 CL E G H524445ORPHA:69665Intrahepatic cholestasis of pregnancyHP:0040284 - Very rare111
HP:0012164HP:0012164Asterixis0ATP8B1 CL E G H52053706ORPHA:69665Intrahepatic cholestasis of pregnancyHP:0040284 - Very rare144
HP:0012164HP:0012164Asterixis0NR1H4 CL E G H99717967ORPHA:69665Intrahepatic cholestasis of pregnancyHP:0040284 - Very rare14
HP:0012164HP:0012164Asterixis0SLC25A13 CL E G H1016510983ORPHA:247585Citrullinemia type IIHP:0040282 - Frequent82

Genes (5) :ABCB11 ABCB4 ATP8B1 NR1H4 SLC25A13

Diseases (2) :ORPHA:69665 ORPHA:247585

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