lissencephaly type 1 due to doublecortin gene mutation
human disease
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lissencephaly type 1 due to doublecortin gene mutation
Summary
lissencephaly type 1 due to doublecortin gene mutation is a class of disease[1].
Key Facts
- lissencephaly type 1 due to doublecortin gene mutation's instance of is recorded as class of disease[2].
- lissencephaly type 1 due to doublecortin gene mutation's OMIM ID is recorded as 300067[3].
- lissencephaly type 1 due to doublecortin gene mutation's Orphanet ID is recorded as 2148[4].
- lissencephaly type 1 due to doublecortin gene mutation's NCI Thesaurus ID is recorded as C205645[5].
- lissencephaly type 1 due to doublecortin gene mutation's genetic association is recorded as DCX[6].
- lissencephaly type 1 due to doublecortin gene mutation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2148[7].
- lissencephaly type 1 due to doublecortin gene mutation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99796[8].
- lissencephaly type 1 due to doublecortin gene mutation's UMLS CUI is recorded as C1848201[9].
- lissencephaly type 1 due to doublecortin gene mutation's UMLS CUI is recorded as C1848199[10].
- lissencephaly type 1 due to doublecortin gene mutation's UMLS CUI is recorded as C1848200[11].
- lissencephaly type 1 due to doublecortin gene mutation's UMLS CUI is recorded as C1848070[12].
- lissencephaly type 1 due to doublecortin gene mutation's ICD-10-CM is recorded as Q04.3[13].
- lissencephaly type 1 due to doublecortin gene mutation's GARD rare disease ID is recorded as 6914[14].
- lissencephaly type 1 due to doublecortin gene mutation's Mondo ID is recorded as MONDO_0010239[15].