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lethal infantile mitochondrial myopathy
human disease
LIMD
MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE
Lethal infantile mitochondrial disease
LIMM
MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE; LIMM
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Statements
instance of
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
class of disease
0 references
subclass of
maternally-inherited mitochondrial myopathy
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
mitochondrial myopathy
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
exact match
http://purl.obolibrary.org/obo/HP_0009069
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009069
http://www.orpha.net/ORDO/Orphanet_254857
0 references
Identifiers
MeSH descriptor ID
C564017
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
C564017
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009069
Human Phenotype Ontology ID
HP:0009069
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009069
ICD-10-CM
G71.3
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
Mondo ID
MONDO_0010792
0 references
OMIM ID
551000
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
Orphanet ID
254857
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
UMLS CUI
C1838876
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0010792
C1838876
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0009069
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