Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abnormality of the nervous system (HP:0000707)help
..Starting node
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Abnormal nervous system physiology (HP:0012638)help
Term ID: 12638
Name: Abnormal nervous system physiology
Synonym: Abnormality of nervous system physiology
Definition: A functional anomaly of the nervous system.
Comments:
Reference: HP:0012638
Genes and Diseases:There are 1269 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandAbnormality of taste sensation (HP:0000223) help
................... HP:0000224 Decreased taste sensation
................... HP:0031249 Parageusia
........expandBehavioral abnormality (HP:0000708) help
................... HP:0000613 Photophobia
................... HP:0000709 Psychosis
................... HP:0000710 Hyperorality
................... HP:0000711 Restlessness
................... HP:0000721 Lack of spontaneous play
................... HP:0000722 Obsessive-compulsive behavior
................... HP:0000729 Autistic behavior
................... HP:0000732 Inflexible adherence to routines or rituals
................... HP:0000736 Short attention span
................... HP:0000738 Hallucinations
................... HP:0000744 Low frustration tolerance
................... HP:0000746 Delusions
................... HP:0000751 Personality changes
................... HP:0000757 Lack of insight
................... HP:0002193 Pseudobulbar behavioral symptoms
................... HP:0002300 Mutism
................... HP:0002307 Drooling
................... HP:0002360 Sleep disturbance
................... HP:0010529 Echolalia
................... HP:0010865 Oppositional defiant disorder
................... HP:0012433 Abnormal social behavior
................... HP:0025112 Sound sensitivity
................... HP:0025160 Abnormal temper tantrums
................... HP:0025356 Pschomotor retardation
................... HP:0025479 Self-neglect
................... HP:0030223 Perseveration
................... HP:0030858 Addictive behavior
................... HP:0031466 Impairment in personality functioning
................... HP:0040202 Abnormal consumption behavior
................... HP:0100753 Schizophrenia
................... HP:0100754 Mania
................... HP:0100851 Abnormal emotion/affect behavior
........expandSeizures (HP:0001250) help
................... HP:0002133 Status epilepticus
................... HP:0002197 Generalized seizures
................... HP:0002373 Febrile seizures
................... HP:0007359 Focal seizures
................... HP:0011097 Epileptic spasms
................... HP:0011145 Symptomatic seizures
................... HP:0011146 Dialeptic seizures
................... HP:0031165 Multifocal seizures
........expandBulbar palsy (HP:0001283) help
........expandEncephalopathy (HP:0001298) help
................... HP:0002448 Progressive encephalopathy
................... HP:0002480 Hepatic encephalopathy
................... HP:0006789 Mitochondrial encephalopathy
................... HP:0006846 Acute encephalopathy
................... HP:0006929 Hypoglycemic encephalopathy
................... HP:0006976 Necrotizing encephalopathy
................... HP:0007030 Nonprogressive encephalopathy
................... HP:0007105 Infantile encephalopathy
................... HP:0007239 Congenital encephalopathy
................... HP:0007335 Recurrent encephalopathy
................... HP:0200134 Epileptic encephalopathy
........expandAbnormal nervous system electrophysiology (HP:0001311) help
................... HP:0030177 Abnormality of peripheral nervous system electrophysiology
................... HP:0030178 Abnormality of central nervous system electrophysiology
........expandDysphagia (HP:0002015) help
................... HP:0002068 Neuromuscular dysphagia
................... HP:0007024 Pseudobulbar paralysis
................... HP:0031146 Impaired oral bolus formation
................... HP:0031162 Impaired oropharyngeal swallow response
................... HP:0200136 Oral-pharyngeal dysphagia
........expandPseudobulbar signs (HP:0002200) help
................... HP:0002193 Pseudobulbar behavioral symptoms
................... HP:0007024 Pseudobulbar paralysis
........expandHeadache (HP:0002315) help
................... HP:0002076 Migraine
................... HP:0002331 Recurrent paroxysmal headache
................... HP:0012199 Cluster headache
................... HP:0012228 Tension-type headache
................... HP:0012318 Occipital neuralgia
................... HP:0012459 Hypnic headache
................... HP:0030907 Thunderclap headache
........expandBulbar signs (HP:0002483) help
........expandCataplexy (HP:0002524) help
........expandEasy fatigability (HP:0003388) help
........expandHypocalcemic tetany (HP:0003472) help
........expandAbnormality of the sense of smell (HP:0004408) help
................... HP:0000458 Anosmia
................... HP:0004409 Hyposmia
........expandAbnormality of central motor function (HP:0011442) help
................... HP:0000473 Torticollis
................... HP:0002063 Rigidity
................... HP:0002071 Abnormality of extrapyramidal motor function
................... HP:0002186 Apraxia
................... HP:0002493 Upper motor neuron dysfunction
................... HP:0003470 Paralysis
................... HP:0011398 Central hypotonia
................... HP:0011443 Abnormality of coordination
................... HP:0012079 Abnormality of central motor conduction
................... HP:0100021 Cerebral palsy
........expandAbnormality of higher mental function (HP:0011446) help
................... HP:0002167 Neurological speech impairment
................... HP:0002186 Apraxia
................... HP:0002463 Language impairment
................... HP:0004372 Reduced consciousness/confusion
................... HP:0010524 Agnosia
................... HP:0031868 Optic ataxia
................... HP:0031908 Micrographia
................... HP:0100543 Cognitive impairment
........expandAbnormality of central sensory function (HP:0011730) help
................... HP:0010527 Astereognosia
................... HP:0011810 Impaired two-point discrimination
................... HP:0011811 Impaired touch localization
................... HP:0011812 Agraphesthesia
........expandAbnormal hypothalamus physiology (HP:0012285) help
................... HP:0003164 Hypothalamic gonadotropin-releasing hormone deficiency
................... HP:0008237 Hypothalamic hypothyroidism
................... HP:0012287 Hypothalamic luteinizing hormone-releasing hormone deficiency
........expandAbnormal synaptic transmission (HP:0012535) help
................... HP:0030191 Abnormal peripheral nervous system synaptic transmission
........expandAbnormality of intracranial pressure (HP:0012640) help
................... HP:0002516 Increased intracranial pressure
................... HP:0012641 Decreased intracranial pressure
........expandAbnormal brain positron emission tomography (HP:0012657) help
................... HP:0012658 Abnormal brain FDG positron emission tomography
........expandAbnormality of pineal physiology (HP:0012688) help
................... HP:0012689 Abnormal pineal melatonin secretion
........expandAbnormal metabolic brain imaging by MRS (HP:0012705) help
................... HP:0012709 Abnormal brain choline/creatine ratio by MRS
................... HP:0025045 Abnormal brain lactate level by MRS
................... HP:0025047 Abnormal brain choline level by MRS
................... HP:0025049 Abnormal brain creatine level by MRS
................... HP:0025052 Abnormal brain N-acetyl aspartate level by MRS
................... HP:0025460 High myoinositol in brain by MRS
................... HP:0030980 Reduced brain glutamine level by MRS
................... HP:0031161 Reduced brain glutamate level by MRS
................... HP:0500021 Reduced brain gamma-aminobutyric acid level by MRS
........expandNeurodevelopmental abnormality (HP:0012759) help
................... HP:0001249 Intellectual disability
................... HP:0001328 Specific learning disability
................... HP:0002376 Developmental regression
................... HP:0007281 Developmental stagnation
................... HP:0012758 Neurodevelopmental delay
........expandAbnormality of movement (HP:0100022) help
................... HP:0000743 Frontal release signs
................... HP:0000752 Hyperactivity
................... HP:0001288 Gait disturbance
................... HP:0001332 Dystonia
................... HP:0001335 Bimanual synkinesia
................... HP:0002172 Postural instability
................... HP:0002374 Diminished movement
................... HP:0002411 Myokymia
................... HP:0002457 Abnormal head movements
................... HP:0002476 Primitive reflex
................... HP:0002487 Hyperkinesis
................... HP:0002533 Abnormal posturing
................... HP:0004305 Involuntary movements
................... HP:0010546 Muscle fibrillation
................... HP:0012164 Asterixis
................... HP:0020037 Astasia
................... HP:0025403 Stooped posture
................... HP:0031826 Abnormal reflex
................... HP:0100021 Cerebral palsy
................... HP:0100660 Dyskinesia

 Sister Nodes: 
..expandAbnormal nervous system morphology (HP:0012639) help
..expandAbnormality of ganglion (HP:0410014) help
..expandAbnormality of the peripheral nervous system (HP:0410008) help


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.