Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the nervous system (HP:0000707)help
Parent Node:
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Abnormal nervous system morphology (HP:0012639)help
..Starting node
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Morphological central nervous system abnormality (HP:0002011)help
Term ID: 2011
Name: Morphological central nervous system abnormality
Synonym: Abnormality of the central nervous system; Central nervous system disease; Morphological abnormality of the central nervous system; Morphological abnormality of the CNS
Definition: A structural abnormality of the central nervous system.
Comments:
Reference: HP:0002011
Genes and Diseases:There are 782 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandMorphological abnormality of the pyramidal tract (HP:0002062) help
................... HP:0002492 Abnormality of the corticospinal tract
................... HP:0007363 Aplasia/Hypoplasia of the pyramidal tract
........expandEncephalocele (HP:0002084) help
................... HP:0002085 Occipital encephalocele
................... HP:0004423 Cranium bifidum occultum
................... HP:0006888 Meningoencephalocele
................... HP:0006992 Anterior basal encephalocele
................... HP:0007035 Anterior encephalocele
................... HP:0007115 Orbital encephalocele
................... HP:0007330 Frontal encephalocele
................... HP:0011816 Parietal encephalocele
................... HP:0011817 Basal encephalocele
........expandAbnormality of the spinal cord (HP:0002143) help
................... HP:0002144 Tethered cord
................... HP:0002176 Spinal cord compression
................... HP:0002196 Myelopathy
................... HP:0002390 Spinal arteriovenous malformation
................... HP:0002423 Long-tract signs
................... HP:0003133 Abnormality of the spinocerebellar tracts
................... HP:0007344 Atrophy/Degeneration involving the spinal cord
................... HP:0008311 Spinal cord posterior columns myelin loss
................... HP:0010301 Spinal dysraphism
................... HP:0010302 Spinal cord tumor
................... HP:0010303 Abnormality of the spinal meninges
................... HP:0011397 Abnormality of the dorsal column of the spinal cord
................... HP:0012486 Myelitis
................... HP:0030325 Cervicomedullary schisis
................... HP:0040272 Hyperintensity of MRI T2 signal of the spinal cord
................... HP:0100561 Spinal cord lesion
........expandAbnormality of neuronal migration (HP:0002269) help
................... HP:0002282 Heterotopia
................... HP:0002536 Abnormal cortical gyration
........expandAlzheimer disease (HP:0002511) help
........expandAbnormality of the cerebrospinal fluid (HP:0002921) help
................... HP:0000238 Hydrocephalus
................... HP:0012229 CSF pleocytosis
................... HP:0012510 Extra-axial cerebrospinal fluid accumulation
................... HP:0025454 Abnormal CSF metabolite level
................... HP:0025456 Abnormal CSF protein level
................... HP:0030981 Abnormal CSF/serum albumin ratio
................... HP:0030998 Cerebrospinal fluid rhinorrhoea
........expandAplasia/Hypoplasia involving the central nervous system (HP:0002977) help
................... HP:0000609 Optic nerve hypoplasia
................... HP:0002283 Global brain atrophy
................... HP:0006894 Hypoplastic olfactory lobes
................... HP:0007036 Hypoplasia of olfactory tract
................... HP:0007360 Aplasia/Hypoplasia of the cerebellum
................... HP:0007362 Aplasia/Hypoplasia of the brainstem
................... HP:0007363 Aplasia/Hypoplasia of the pyramidal tract
................... HP:0007364 Aplasia/Hypoplasia of the cerebrum
................... HP:0007365 Aplasia/Hypoplasia involving the corticospinal tracts
................... HP:0007369 Atrophy/Degeneration affecting the cerebrum
................... HP:0011000 Aplasia/Hypoplasia of the optic tract
................... HP:0012687 Agenesis of pineal gland
................... HP:0040326 Hypoplasia of the olfactory bulb
........expandAtrophy/Degeneration affecting the central nervous system (HP:0007367) help
................... HP:0002180 Neurodegeneration
................... HP:0002529 Neuronal loss in central nervous system
................... HP:0007009 Central nervous system degeneration
................... HP:0007344 Atrophy/Degeneration involving the spinal cord
................... HP:0007366 Atrophy/Degeneration affecting the brainstem
................... HP:0007372 Atrophy/Degeneration involving the corticospinal tracts
................... HP:0007373 Motor neuron atrophy
................... HP:0011813 Increased cerebral lipofuscin
................... HP:0012444 Brain atrophy
................... HP:0100256 Senile plaques
........expandAbnormality of the meninges (HP:0010651) help
................... HP:0002435 Meningocele
................... HP:0010303 Abnormality of the spinal meninges
................... HP:0010652 Abnormality of the dura mater
................... HP:0100250 Meningeal calcification
................... HP:0100700 Abnormality of the arachnoid mater
................... HP:0100701 Abnormality of the pia mater
........expandAbnormal CNS myelination (HP:0011400) help
................... HP:0002188 Delayed CNS myelination
................... HP:0002415 Leukodystrophy
................... HP:0003429 CNS hypomyelination
................... HP:0007266 Cerebral dysmyelination
................... HP:0007305 CNS demyelination
................... HP:0012754 CNS hypermyelination
........expandCNS infection (HP:0011450) help
................... HP:0001287 Meningitis
................... HP:0002383 Encephalitis
................... HP:0006946 Recurrent meningitis
................... HP:0030049 Brain abscess
........expandAbnormality of brain morphology (HP:0012443) help
................... HP:0001322 Brain very small
................... HP:0001343 Kernicterus
................... HP:0001360 Holoprosencephaly
................... HP:0002118 Abnormality of the cerebral ventricles
................... HP:0002363 Abnormality of brainstem morphology
................... HP:0002418 Abnormality of midbrain morphology
................... HP:0011282 Abnormality of hindbrain morphology
................... HP:0012503 Abnormality of the pituitary gland
................... HP:0012675 Iron accumulation in brain
................... HP:0012676 Copper accumulation in brain
................... HP:0012681 Abnormality of pineal morphology
................... HP:0100547 Abnormality of forebrain morphology
................... HP:0100659 Abnormality of the cerebral vasculature
........expandAbnormality of the subarachnoid space (HP:0012703) help
................... HP:0002138 Subarachnoid hemorrhage
................... HP:0012704 Widened subarachnoid space
........expandCentral nervous system cyst (HP:0030724) help
................... HP:0010576 Intracranial cystic lesion
................... HP:0030725 Neurenteric cyst
........expandNeoplasm of the central nervous system (HP:0100006) help
................... HP:0010302 Spinal cord tumor
................... HP:0025170 Neuronal/glioneuronal neoplasm of the central nervous system
................... HP:0030692 Brain neoplasm
................... HP:0100835 Benign neoplasm of the central nervous system
................... HP:0100836 Malignant neoplasm of the central nervous system
........expandAbnormality of the glial cells (HP:0100705) help
................... HP:0002171 Gliosis
................... HP:0002446 Astrocytosis
................... HP:0009733 Glioma
................... HP:0100706 Abnormality of the oligodendroglia
................... HP:0100707 Abnormality of the astrocytes
................... HP:0100708 Abnormality of the microglia
........expandAbnormal neural tube morphology (HP:0410043) help
................... HP:0045005 Neural tube defect

 Sister Nodes: 
..expandAbnormal myelination (HP:0012447) help
..expandAbnormal neuron morphology (HP:0012757) help
..expandAbnormal peripheral nervous system morphology (HP:0000759) help
..expandNeoplasm of the nervous system (HP:0004375) 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.