An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.
Attributes | Values |
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rdf:type | |
description |
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exact match | |
exact match | |
Mondo ID | |
Disease Ontology ID | |
Mondo ID | |
Disease Ontology ID | |
Mondo ID |
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Disease Ontology ID |
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rdfs:label |
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skos:prefLabel |
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name |
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instance of | |
instance of | |
subclass of | |
subclass of | |
ICD-10-CM | |
OMIM ID | |
ICD-10-CM |
|
OMIM ID |
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skos:altLabel |
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UMLS CUI | |
on focus list of Wikimedia project | |
UMLS CUI |
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on focus list of Wikimedia project | |
is about of |