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: ..Coma (HP:0001259) ..Confusion (HP:0001289) ..Drowsiness (HP:0002329) ..Episodic hypersomnia (HP:0007200) ..Excessive daytime somnolence (HP:0001262) ..Fluctuations in consciousness (HP:0007159) ..Lethargy (HP:0001254) ..Loss of consciousness (HP:0007185) ..obsolete Excessive daytime sleepiness (HP:0002189) Input HPO ID HPO term Distance Gene Gene id entrez HGNC ID DiseaseId DiseaseName Frequency Onset HGMD variants ClinVar variants HPO disease - gene - phenotype typical associations: HPO disease - gene - phenotype less frequent non-typical associations: HP:0031358 HP:0031358 Vegetative state 0 AARS1 CL E G H 16 20 OMIM:619661 LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2; HDLS2 HP:0031358 HP:0031358 Vegetative state 0 ABCD1 CL E G H 215 61 ORPHA:139396 X-linked cerebral adrenoleukodystrophy HP:0040284 - Very rare 135 HP:0031358 HP:0031358 Vegetative state 0 ARSA CL E G H 410 713 ORPHA:309271 Metachromatic leukodystrophy, adult form HP:0040284 - Very rare 253 HP:0031358 HP:0031358 Vegetative state 0 ARSA CL E G H 410 713 ORPHA:309263 Metachromatic leukodystrophy, juvenile form HP:0040284 - Very rare 253 HP:0031358 HP:0031358 Vegetative state 0 ARSA CL E G H 410 713 ORPHA:309256 Metachromatic leukodystrophy, late infantile form HP:0040284 - Very rare 253 HP:0031358 HP:0031358 Vegetative state 0 EPM2A CL E G H 7957 3413 ORPHA:501 Lafora disease HP:0040283 - Occasional 83 HP:0031358 HP:0031358 Vegetative state 0 ISCA2 CL E G H 122961 19857 OMIM:616370 Multiple mitochondrial dysfunctions syndrome 4 . 7 HP:0031358 HP:0031358 Vegetative state 0 NHLRC1 CL E G H 378884 21576 ORPHA:501 Lafora disease HP:0040283 - Occasional 77 HP:0031358 HP:0031358 Vegetative state 0 PIGA CL E G H 5277 8957 OMIM:301072 NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS; NEDEPH 46 HP:0031358 HP:0031358 Vegetative state 0 PLA2G6 CL E G H 8398 9039 ORPHA:35069 Infantile neuroaxonal dystrophy HP:0040284 - Very rare 133 HP:0031358 HP:0031358 Vegetative state 0 PSAP CL E G H 5660 9498 OMIM:611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY 81 HP:0031358 HP:0031358 Vegetative state 0 PSAP CL E G H 5660 9498 ORPHA:309271 Metachromatic leukodystrophy, adult form HP:0040284 - Very rare 81 HP:0031358 HP:0031358 Vegetative state 0 PSAP CL E G H 5660 9498 ORPHA:309263 Metachromatic leukodystrophy, juvenile form HP:0040284 - Very rare 81 HP:0031358 HP:0031358 Vegetative state 0 PSAP CL E G H 5660 9498 ORPHA:309256 Metachromatic leukodystrophy, late infantile form HP:0040284 - Very rare 81 HP:0031358 HP:0031358 Vegetative state 0 SHQ1 CL E G H 55164 25543 OMIM:619922 HP:0031358 HP:0031358 Vegetative state 0 TTC26 CL E G H 79989 21882 OMIM:619534 BILIARY, 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.