Human Phenotype
Ontology
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Grandparent Node: Myelopathy (HP:0002196) |
Parent Node: Cervical myelopathy (HP:0002318) |
..Starting node ..Abnormal cervical myelogram (HP:0005788)
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Term ID: |
5788 |
Name: |
Abnormal cervical myelogram |
Synonym: |
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Definition: |
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Comments: |
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Reference: |
HP:0005788 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0005788 | HP:0005788 | Abnormal cervical myelogram | 0 | CL E G H | | | | | | | | | | |
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.
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