Human Phenotype Ontology 
Grandparent Node:
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Abnormality of higher mental function (HP:0011446)help
Parent Node:
expand
Reduced consciousness/confusion (HP:0004372)help
..Starting node
..expand
Vegetative state (HP:0031358)help
Term ID: 31358
Name: Vegetative state
Synonym:
Definition: Absence of wakefulness and conscience, but (in contrast to coma) with involuntary opening of the eyes and movements (such as teeth grinding, yawning, or thrashing of the extremities).
Comments:
Reference: HP:0031358
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandComa (HP:0001259) help
..expandConfusion (HP:0001289) help
..expandDrowsiness (HP:0002329) help
..expandEpisodic hypersomnia (HP:0007200) help
..expandExcessive daytime somnolence (HP:0001262) help
..expandFluctuations in consciousness (HP:0007159) help
..expandLethargy (HP:0001254) help
..expandLoss of consciousness (HP:0007185) help
..expandobsolete Excessive daytime sleepiness (HP:0002189) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031358HP:0031358Vegetative state0AARS1 CL E G H1620OMIM:619661LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2; HDLS2
HP:0031358HP:0031358Vegetative state0ABCD1 CL E G H21561ORPHA:139396X-linked cerebral adrenoleukodystrophyHP:0040284 - Very rare135
HP:0031358HP:0031358Vegetative state0ARSA CL E G H410713ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare253
HP:0031358HP:0031358Vegetative state0ARSA CL E G H410713ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040284 - Very rare253
HP:0031358HP:0031358Vegetative state0ARSA CL E G H410713ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040284 - Very rare253
HP:0031358HP:0031358Vegetative state0EPM2A CL E G H79573413ORPHA:501Lafora diseaseHP:0040283 - Occasional83
HP:0031358HP:0031358Vegetative state0ISCA2 CL E G H12296119857OMIM:616370Multiple mitochondrial dysfunctions syndrome 4.7
HP:0031358HP:0031358Vegetative state0NHLRC1 CL E G H37888421576ORPHA:501Lafora diseaseHP:0040283 - Occasional77
HP:0031358HP:0031358Vegetative state0PIGA CL E G H52778957OMIM:301072NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS; NEDEPH46
HP:0031358HP:0031358Vegetative state0PLA2G6 CL E G H83989039ORPHA:35069Infantile neuroaxonal dystrophyHP:0040284 - Very rare133
HP:0031358HP:0031358Vegetative state0PSAP CL E G H56609498OMIM:611722KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY81
HP:0031358HP:0031358Vegetative state0PSAP CL E G H56609498ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare81
HP:0031358HP:0031358Vegetative state0PSAP CL E G H56609498ORPHA:309263Metachromatic leukodystrophy, juvenile formHP:0040284 - Very rare81
HP:0031358HP:0031358Vegetative state0PSAP CL E G H56609498ORPHA:309256Metachromatic leukodystrophy, late infantile formHP:0040284 - Very rare81
HP:0031358HP:0031358Vegetative state0SHQ1 CL E G H5516425543OMIM:619922
HP:0031358HP:0031358Vegetative state0TTC26 CL E G H7998921882OMIM:619534BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME; BRENS


Genes (11) :AARS1 ABCD1 ARSA EPM2A ISCA2 NHLRC1 PIGA PLA2G6 PSAP SHQ1 TTC26

Diseases (12) :OMIM:619661 ORPHA:139396 ORPHA:309271 ORPHA:309263 ORPHA:309256 ORPHA:501 OMIM:616370 OMIM:301072 ORPHA:35069 OMIM:611722 OMIM:619922 OMIM:619534
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.