autosomal dominant mental retardation 56
human disease
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Summary
autosomal dominant mental retardation 56 is a class of disease[1].
Key Facts
- autosomal dominant mental retardation 56's instance of is recorded as class of disease[2].
- autosomal dominant mental retardation 56's subclass of is recorded as autosomal dominant disease[3].
- autosomal dominant mental retardation 56's subclass of is recorded as syndromic intellectual disability[4].
- autosomal dominant mental retardation 56's OMIM ID is recorded as 617854[5].
- autosomal dominant mental retardation 56's Disease Ontology ID is recorded as DOID:0080226[6].
- autosomal dominant mental retardation 56's Orphanet ID is recorded as 178469[7].
- autosomal dominant mental retardation 56's Orphanet ID is recorded as 442835[8].
- autosomal dominant mental retardation 56's genetic association is recorded as CLTC[9].
- autosomal dominant mental retardation 56's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080226[10].
- autosomal dominant mental retardation 56's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_178469[11].
- autosomal dominant mental retardation 56's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_442835[12].
- autosomal dominant mental retardation 56's exact match is recorded as http://identifiers.org/doid/DOID:0080226[13].
- autosomal dominant mental retardation 56's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant mental retardation 56's Mondo ID is recorded as MONDO_0030922[15].
- autosomal dominant mental retardation 56's UniProt disease ID is recorded as DI-05186[16].