autosomal dominant non-syndromic intellectual disability 8
autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3
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autosomal dominant non-syndromic intellectual disability 8
Summary
autosomal dominant non-syndromic intellectual disability 8 is a rare disease[1].
Key Facts
- autosomal dominant non-syndromic intellectual disability 8's instance of is recorded as rare disease[2].
- autosomal dominant non-syndromic intellectual disability 8's instance of is recorded as class of disease[3].
- autosomal dominant non-syndromic intellectual disability 8's subclass of is recorded as autosomal dominant non-syndromic intellectual disability[4].
- autosomal dominant non-syndromic intellectual disability 8's OMIM ID is recorded as 614254[5].
- autosomal dominant non-syndromic intellectual disability 8's Disease Ontology ID is recorded as DOID:0070038[6].
- autosomal dominant non-syndromic intellectual disability 8's genetic association is recorded as GRIN1[7].
- autosomal dominant non-syndromic intellectual disability 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070038[8].
- autosomal dominant non-syndromic intellectual disability 8's exact match is recorded as http://identifiers.org/doid/DOID:0070038[9].
- autosomal dominant non-syndromic intellectual disability 8's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_178469[10].
- autosomal dominant non-syndromic intellectual disability 8's UMLS CUI is recorded as C3280282[11].
- autosomal dominant non-syndromic intellectual disability 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- autosomal dominant non-syndromic intellectual disability 8's Mondo ID is recorded as MONDO_0013655[13].
- autosomal dominant non-syndromic intellectual disability 8's UniProt disease ID is recorded as DI-05176[14].