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Cell Culture Ontology
Last uploaded:
July 23, 2014
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Preferred Name | complex neurodevelopmental disorder with motor features | |
Synonyms |
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Definitions |
A complex neurodevelopmental disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy). Additionally, the disorder features at least one phenotype associated with motor function, including but not limited to spasticity, hypo- or hypertonia, dyskinesia, choreo-athetosis, or ataxia. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0100516 |
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curated_content_resource |
https://search.clinicalgenome.org/kb/conditions/MONDO:0100516 |
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definition |
A complex neurodevelopmental disorder that involves more than one phenotype associated with the central nervous system, including but not limited to intellectual disability, autism, and seizures (epilepsy). Additionally, the disorder features at least one phenotype associated with motor function, including but not limited to spasticity, hypo- or hypertonia, dyskinesia, choreo-athetosis, or ataxia.
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id |
MONDO:0100516
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in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#clingen http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#inferred_rare |
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label |
complex neurodevelopmental disorder with motor features
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notation |
MONDO:0100516
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preferred label |
complex neurodevelopmental disorder with motor features
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prefLabel |
complex neurodevelopmental disorder with motor features
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terms_creator | ||
subClassOf |
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Mapping To | Ontology | Source |
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http://purl.obolibrary.org/obo/MONDO_0100516 | MONDO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0100516 | EFO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0100516 | DOVES | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0100516 | MONDO | LOOM |
http://purl.obolibrary.org/obo/MONDO_0100516 | EFO | LOOM |
http://purl.obolibrary.org/obo/MONDO_0100516 | DOVES | LOOM |