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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.

Term:Morphological central nervous system abnormality
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Accession:HP:0002011 term browser browse the term
Definition:A structural abnormality of the central nervous system.
Synonyms:exact_synonym: Abnormality of the central nervous system;   Morphological abnormality of the CNS;   Morphological abnormality of the central nervous system
 related_synonym: Central nervous system disease
 alt_id: HP:0002405;   HP:0002413;   HP:0002481;   HP:0007319
 xref: MESH:D002493;   SNOMEDCT_US:23853001;   UMLS:C0007682;   UMLS:C4021765


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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the nervous system 0
        Abnormal nervous system morphology 0
          Morphological central nervous system abnormality 0
            Abnormal CNS myelination + 0
            Abnormal glial cell morphology + 0
            Abnormal meningeal morphology + 0
            Abnormal neural tube morphology + 0
            Abnormal subarachnoid space morphology + 0
            Abnormality of brain morphology + 0
            Abnormality of neuronal migration + 0
            Abnormality of the cerebrospinal fluid + 0
            Abnormality of the spinal cord + 0
            Alzheimer disease 0
            Aplasia/Hypoplasia involving the central nervous system + 0
            Atrophy/Degeneration affecting the central nervous system + 0
            Central nervous system axonal spheroid 0
            Central nervous system cyst + 0
            Morphological abnormality of the pyramidal tract + 0
            Neoplasm of the central nervous system + 0
            Unusual CNS infection + 0
paths to the root