Human Phenotype Ontology 
Grandparent Node:
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Abnormal CSF metabolite level (HP:0025454)help
Parent Node:
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Abnormal CSF glucose level (HP:0031884)help
..Starting node
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Hypoglycorrhachia (HP:0011972)help
Term ID: 11972
Name: Hypoglycorrhachia
Synonym: Decreased CSF glucose; Low glucose levels in cerebral spinal fluid
Definition: Abnormally low glucose concentration in the cerebrospinal fluid.
Comments:
Reference: HP:0011972
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHyperglycorrhachia (HP:0031885) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011972HP:0011972Hypoglycorrhachia0SLC2A1 CL E G H651371277ORPHA196511005138140
HP:0011972HP:0011972Hypoglycorrhachia0SLC2A1 CL E G H6513606777GLUT1 deficiency syndrome 1606777CN030711OMIM196511005138140
HP:0011972HP:0011972Hypoglycorrhachia0SLC2A1 CL E G H6513612126GLUT1 deficiency syndrome 2612126C1842534OMIM196511005138140
HP:0011972HP:0011972Hypoglycorrhachia0SLC2A1 CL E G H6513608885Stomatin-deficient cryohydrocytosis with neurologic defects608885C1837206OMIM196511005138140
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :SLC2A1

Diseases (4) :71277 606777 612126 608885
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.