autosomal dominant mental retardation 48
human disease
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autosomal dominant mental retardation 48
Summary
autosomal dominant mental retardation 48 is a class of disease[1].
Key Facts
- autosomal dominant mental retardation 48's instance of is recorded as class of disease[2].
- autosomal dominant mental retardation 48's subclass of is recorded as autosomal dominant non-syndromic intellectual disability[3].
- autosomal dominant mental retardation 48's OMIM ID is recorded as 617751[4].
- autosomal dominant mental retardation 48's Disease Ontology ID is recorded as DOID:0080235[5].
- autosomal dominant mental retardation 48's Orphanet ID is recorded as 500159[6].
- autosomal dominant mental retardation 48's genetic association is recorded as RAC1[7].
- autosomal dominant mental retardation 48's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080235[8].
- autosomal dominant mental retardation 48's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_500159[9].
- autosomal dominant mental retardation 48's exact match is recorded as http://identifiers.org/doid/DOID:0080235[10].
- autosomal dominant mental retardation 48's UMLS CUI is recorded as C4540321[11].
- autosomal dominant mental retardation 48's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal dominant mental retardation 48's Mondo ID is recorded as MONDO_0030913[13].
- autosomal dominant mental retardation 48's UniProt disease ID is recorded as DI-05131[14].
- autosomal dominant mental retardation 48's Experimental Factor Ontology ID is recorded as 0009156[15].