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 morphology (HP:0012639)help
Term ID: 12639
Name: Abnormal nervous system morphology
Synonym: Abnormal shape of nervous system; Abnormality of nervous system morphology
Definition: A structural anomaly of the nervous system.
Comments:
Reference: HP:0012639
Genes and Diseases:There are 1064 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandAbnormal peripheral nervous system morphology (HP:0000759) help
................... HP:0000764 Peripheral axonal degeneration
................... HP:0001291 Abnormality of the cranial nerves
................... HP:0002366 Abnormal lower motor neuron morphology
................... HP:0003009 Enhanced neurotoxicity of vincristine
................... HP:0003130 Abnormal peripheral myelination
................... HP:0003382 Hypertrophic nerve changes
................... HP:0003405 Diffuse axonal swelling
................... HP:0003443 Decreased size of nerve terminals
................... HP:0006802 Abnormal anterior horn cell morphology
................... HP:0009830 Peripheral neuropathy
................... HP:0031001 Minifascicle formation
................... HP:0031002 Neuritis
................... HP:0045010 Abnormality of peripheral nerves
................... HP:0100007 Neoplasm of the peripheral nervous system
........expandMorphological abnormality of the central nervous system (HP:0002011) help
................... HP:0002062 Morphological abnormality of the pyramidal tract
................... HP:0002084 Encephalocele
................... HP:0002143 Abnormality of the spinal cord
................... HP:0002269 Abnormality of neuronal migration
................... HP:0002511 Alzheimer disease
................... HP:0002921 Abnormality of the cerebrospinal fluid
................... HP:0002977 Aplasia/Hypoplasia involving the central nervous system
................... HP:0007367 Atrophy/Degeneration affecting the central nervous system
................... HP:0010651 Abnormality of the meninges
................... HP:0011400 Abnormal CNS myelination
................... HP:0011450 CNS infection
................... HP:0012443 Abnormality of brain morphology
................... HP:0012703 Abnormality of the subarachnoid space
................... HP:0030724 Central nervous system cyst
................... HP:0100006 Neoplasm of the central nervous system
................... HP:0100705 Abnormality of the glial cells
................... HP:0410043 Abnormal neural tube morphology
........expandNeoplasm of the nervous system (HP:0004375) help
................... HP:0100006 Neoplasm of the central nervous system
................... HP:0100007 Neoplasm of the peripheral nervous system
........expandAbnormal myelination (HP:0012447) help
................... HP:0003130 Abnormal peripheral myelination
................... HP:0007108 Demyelinating peripheral neuropathy
................... HP:0007327 Mixed demyelinating and axonal polyneuropathy
................... HP:0007922 Hypermyelinated retinal nerve fibers
................... HP:0011400 Abnormal CNS myelination
................... HP:0012448 Delayed myelination
........expandAbnormal neuron morphology (HP:0012757) help
................... HP:0002450 Abnormal motor neuron morphology
................... HP:0500032 Abnormal neuron branching

 Sister Nodes: 
..expandAbnormal nervous system physiology (HP:0012638) 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 December 15 2022 release.