Human Health Exposure Analysis Resource

Last uploaded: July 19, 2024
Preferred Name

MELAS syndrome
Synonyms

MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES

Definitions

A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins. OMIM mapping confirmed by DO. [SN].

ID

http://purl.obolibrary.org/obo/DOID_3687

comment

OMIM mapping confirmed by DO. [SN].

alternative label

MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES

database_cross_reference

UMLS_CUI:C0162671

MESH:D017241

ICD10CM:E88.41

SNOMEDCT_US_2023_03_01:39925003

MIM:540000

NCI:C84885

definition

A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins.

OMIM mapping confirmed by DO. [SN].

has exact synonym

MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES

has symptom

http://purl.obolibrary.org/obo/SYMP_0000504

http://purl.obolibrary.org/obo/SYMP_0000329

http://purl.obolibrary.org/obo/SYMP_0000293

http://purl.obolibrary.org/obo/SYMP_0000124

http://purl.obolibrary.org/obo/SYMP_0000130

has_obo_namespace

disease_ontology

id

DOID:3687

in_subset

http://purl.obolibrary.org/obo/doid#NCIthesaurus

label

MELAS syndrome

notation

DOID:3687

note

A mitochondrial encephalomyopathy that is characterized by mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes, has_symptom myalgia, motor weakness, headaches, seizures, and stroke-like episodes with acute hemiparesis and severe headaches, and develops_from mutation in mitochondrial genes including MT-TL1, which encodes tRNA proteins.

OMIM mapping confirmed by DO. [SN].

preferred label

MELAS syndrome

prefLabel

MELAS syndrome

subClassOf

http://purl.obolibrary.org/obo/DOID_890

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Create mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_3687 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 EPIO SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 DDSS SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 MIDO SAME_URI
http://purl.obolibrary.org/obo/DOID_3687 FNS-H SAME_URI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.660.560.620.520 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.132.100.535 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_63 HRDO LOOM
http://purl.obolibrary.org/obo/NCIT_C84885 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.189.535 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D017241 RH-MESH LOOM
http://id.nlm.nih.gov/mesh/D017241 MDM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.163.100.535 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.651.460.620.520 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#17939 OCHV LOOM
http://purl.obolibrary.org/obo/DOID_3687 DOID LOOM
http://purl.obolibrary.org/obo/DOID_3687 BAO LOOM
http://purl.obolibrary.org/obo/DOID_3687 EPIO LOOM
http://purl.obolibrary.org/obo/DOID_3687 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_3687 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_3687 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_3687 FNS-H LOOM
urn:agi-pathway:uuid-9662419c-8806-40b7-947d-2c6872258caa BPT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.300.275.500 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0017626 OMIT LOOM
http://purl.bioontology.org/ontology/MESH/D017241 MESH LOOM
http://purl.jp/bio/4/id/200906055206482716 IOBC LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038501 PMAPP-PMO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_3687 NATPRO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#MELAS_Syndrome CSEO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84885 NCIT LOOM
http://purl.obolibrary.org/obo/MONDO_0010789 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0010789 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0010789 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0010789 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0010789 DOVES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.189.535 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICD10CM/E88.41 ICD10CM LOOM
http://purl.bioontology.org/ontology/MEDDRA/10053872 MEDDRA LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.491.500.500.500 RH-MESH LOOM
urn:agi-folder:melas_syndrome BPT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.907.253.329.500 RH-MESH LOOM
rgo:24890 GAMUTS LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0162671 OCHV LOOM