Human Phenotype Ontology 
Grandparent Node:
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Abnormal cerebral vascular morphology (HP:0100659)help
Parent Node:
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Stroke (HP:0001297)help
..Starting node
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Stroke-like episode (HP:0002401)help
Term ID: 2401
Name: Stroke-like episode
Synonym: Stroke-like episodes; Strokelike episodes
Definition: No consensus exists on what a stroke-like episode is, but these episodes can be functionally defined as a new neurological deficit, occurring with or without the context of seizures, which last longer than 24 hours.
Comments:
Reference: HP:0002401
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIschemic stroke (HP:0002140) help
..expandTransient ischemic attack (HP:0002326) 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:0002401HP:0002401Stroke-like episode0AMACR CL E G H23600451ORPHA:79095Congenital bile acid synthesis defect type 444
HP:0002401HP:0002401Stroke-like episode0COX1 CL E G H45127419ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0COX1 CL E G H45127419OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0COX2 CL E G H45137421ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0COX2 CL E G H45137421OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0COX3 CL E G H45147422ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0COX3 CL E G H45147422OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0CYTB CL E G H45197427ORPHA:137675Histiocytoid cardiomyopathyHP:0040283 - Occasional
HP:0002401HP:0002401Stroke-like episode0CYTB CL E G H45197427OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0DPAGT1 CL E G H17982995ORPHA:86309DPAGT1-CDGHP:0040284 - Very rare38
HP:0002401HP:0002401Stroke-like episode0DPM3 CL E G H543443007ORPHA:263494DPM3-CDGHP:0040282 - Frequent9
HP:0002401HP:0002401Stroke-like episode0HTRA1 CL E G H56549476ORPHA:199354Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy34
HP:0002401HP:0002401Stroke-like episode0LIG3 CL E G H39806600OMIM:619780MITOCHONDRIAL DNA DEPLETION SYNDROME 20 (MNGIE TYPE); MTDPS201
HP:0002401HP:0002401Stroke-like episode0LRPPRC CL E G H1012815714ORPHA:70472Congenital lactic acidosis, Saguenay-Lac-Saint-Jean typeHP:0040281 - Very frequent191
HP:0002401HP:0002401Stroke-like episode0ND1 CL E G H45357455ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0ND1 CL E G H45357455OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0ND4 CL E G H45387459ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0ND5 CL E G H45407461ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0ND5 CL E G H45407461OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0ND6 CL E G H45417462ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0ND6 CL E G H45417462OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0NDUFA8 CL E G H47027692OMIM:619272MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37; MC1DN37
HP:0002401HP:0002401Stroke-like episode0PMM2 CL E G H53739115OMIM:212065Congenital disorder of glycosylation, type Ia.150
HP:0002401HP:0002401Stroke-like episode0PRNP CL E G H56219449ORPHA:282166Inherited Creutzfeldt-Jakob diseaseHP:0040282 - Frequent69
HP:0002401HP:0002401Stroke-like episode0RFT1 CL E G H9186930220ORPHA:244310RFT1-CDGHP:0040283 - Occasional92
HP:0002401HP:0002401Stroke-like episode0STIM1 CL E G H678611386OMIM:185070Stormorken syndromeHP:0040283 - Occasional31
HP:0002401HP:0002401Stroke-like episode0TRNC CL E G H45117477OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNF CL E G H45587481ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNF CL E G H45587481OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNH CL E G H45647487ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNK CL E G H45667489OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNL1 CL E G H45677490ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNL1 CL E G H45677490OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNQ CL E G H45727495ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNQ CL E G H45727495OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNS1 CL E G H45747497ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNS1 CL E G H45747497OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNS2 CL E G H45757498ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNS2 CL E G H45757498OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNV CL E G H45777500OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TRNW CL E G H45787501ORPHA:550MELASHP:0040281 - Very frequent
HP:0002401HP:0002401Stroke-like episode0TRNW CL E G H45787501OMIM:540000Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
HP:0002401HP:0002401Stroke-like episode0TTR CL E G H727612405OMIM:105210Amyloidosis, hereditary, transthyretin-related.107
HP:0002401HP:0002401Stroke-like episode0WFS1 CL E G H746612762OMIM:222300Wolfram syndrome 1.389


Genes (31) :AMACR COX1 COX2 COX3 CYTB DPAGT1 DPM3 HTRA1 LIG3 LRPPRC ND1 ND4 ND5 ND6 NDUFA8 PMM2 PRNP RFT1 STIM1 TRNC TRNF TRNH TRNK TRNL1 TRNQ TRNS1 TRNS2 TRNV TRNW TTR WFS1

Diseases (16) :ORPHA:79095 ORPHA:550 OMIM:540000 ORPHA:137675 ORPHA:86309 ORPHA:263494 ORPHA:199354 OMIM:619780 ORPHA:70472 OMIM:619272 OMIM:212065 ORPHA:282166 ORPHA:244310 OMIM:185070 OMIM:105210 OMIM:222300
 

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