autosomal dominant mental retardation 46
human disease
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autosomal dominant mental retardation 46
Summary
autosomal dominant mental retardation 46 is a class of disease[1].
Key Facts
- autosomal dominant mental retardation 46's instance of is recorded as class of disease[2].
- autosomal dominant mental retardation 46's subclass of is recorded as autosomal dominant non-syndromic intellectual disability[3].
- autosomal dominant mental retardation 46's OMIM ID is recorded as 617601[4].
- autosomal dominant mental retardation 46's Disease Ontology ID is recorded as DOID:0080237[5].
- autosomal dominant mental retardation 46's genetic association is recorded as KCNQ5[6].
- autosomal dominant mental retardation 46's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080237[7].
- autosomal dominant mental retardation 46's exact match is recorded as http://identifiers.org/doid/DOID:0080237[8].
- autosomal dominant mental retardation 46's UMLS CUI is recorded as C4539851[9].
- autosomal dominant mental retardation 46's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
- autosomal dominant mental retardation 46's Mondo ID is recorded as MONDO_0030911[11].
- autosomal dominant mental retardation 46's UniProt disease ID is recorded as DI-05062[12].