Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the cerebrospinal fluid (HP:0002921)help
Parent Node:
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Abnormal CSF metabolite level (HP:0025454)help
..Starting node
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Abnormal CSF dopamine level (HP:0012654)help
Term ID: 12654
Name: Abnormal CSF dopamine level
Synonym:
Definition: Abnormal concentration of dopamine in the cerebrospinal fluid (CSF).
Comments:
Reference: HP:0012654
Genes and Diseases:
 
       Child Nodes:
........expandElevated CSF dopamine level (HP:0012655) help
........expandReduced CSF dopamine level (HP:0012656) help

 Sister Nodes: 
..expandAbnormal CSF biopterin level (HP:0040207) help
..expandAbnormal CSF glucose level (HP:0031884) help
..expandAbnormal CSF lactate level (HP:0030085) help
..expandAbnormal CSF neopterin level (HP:0040203) help
..expandDecreased CSF 5-hydroxyindolacetic acid (HP:0025455) help
..expandDecreased CSF 5-methyltetrahydrofolate concentration (HP:0012446) help
..expandDecreased CSF homovanillic acid (HP:0003785) help
..expandDecreased level of erythritol in CSF (HP:0410056) help
..expandIncreased CSF interferon alpha (HP:0009709) help
..expandIncreased level of D-threitol in CSF (HP:0410058) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012654HP:0012654Abnormal CSF dopamine level0 CL E G H
HP:0012654HP:0012656Reduced CSF dopamine level1 CL E G H
HP:0012654HP:0012655Elevated CSF dopamine level1 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 August 2021 release.