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Preferred term label: Catatonia
Synonyms Catalepsy
Definition (free text, please give PubMed ID) Neuropsychiatric syndrome associated with severe mental illness, commonly involving abnormal movements and behaviors such as stupor, catalepsy, waxy flexibility, mutism, negativism, posturing, mannerisms, stereotypy, and agitation. PubMed ID: 28613592
Parent term (use hpo.jax.org/app) Abnormal nervous system physiology, HP:0012638
Diseases characterized by this term ? (e.g. Orphanet or OMIM number) Schizophrenia, OMIM:181500 (https://omim.org/entry/181500) Schizophrenia 10, OMIM: 605419 Epilepsy, nocturnal frontal lobe, 5, OMIM: 615005 Kleefstra syndrome, OMIM:610253 (https://omim.org/entry/610253) Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay, OMIM:616539 (https://omim.org/entry/616539) Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, OMIM:618124 (https://omim.org/entry/618124) Neuroleptic malignant syndrome, ORPHA:94093 (https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=94093) NMDA receptor encephalitis, ORPHA:217253 (https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=217253)
Your nano-attribution (ORCID) 0000-0003-1909-0010
The text was updated successfully, but these errors were encountered:
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Preferred term label:
Catatonia
Synonyms
Catalepsy
Definition (free text, please give PubMed ID)
Neuropsychiatric syndrome associated with severe mental illness, commonly involving abnormal movements and behaviors such as stupor, catalepsy, waxy flexibility, mutism, negativism, posturing, mannerisms, stereotypy, and agitation.
PubMed ID: 28613592
Parent term (use hpo.jax.org/app)
Abnormal nervous system physiology, HP:0012638
Diseases characterized by this term ? (e.g. Orphanet or OMIM number)
Schizophrenia, OMIM:181500 (https://omim.org/entry/181500)
Schizophrenia 10, OMIM: 605419
Epilepsy, nocturnal frontal lobe, 5, OMIM: 615005
Kleefstra syndrome, OMIM:610253 (https://omim.org/entry/610253)
Peripheral neuropathy with variable spasticity, exercise intolerance, and developmental delay, OMIM:616539 (https://omim.org/entry/616539)
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development, OMIM:618124 (https://omim.org/entry/618124)
Neuroleptic malignant syndrome, ORPHA:94093 (https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=94093)
NMDA receptor encephalitis, ORPHA:217253 (https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=217253)
Your nano-attribution (ORCID)
0000-0003-1909-0010
The text was updated successfully, but these errors were encountered: