lissencephaly due to LIS1 mutation
human disease
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lissencephaly due to LIS1 mutation
Summary
lissencephaly due to LIS1 mutation is a class of disease[1].
Key Facts
- lissencephaly due to LIS1 mutation's instance of is recorded as class of disease[2].
- lissencephaly due to LIS1 mutation's subclass of is recorded as classic lissencephaly[3].
- lissencephaly due to LIS1 mutation's OMIM ID is recorded as 607432[4].
- lissencephaly due to LIS1 mutation's Orphanet ID is recorded as 95232[5].
- lissencephaly due to LIS1 mutation's genetic association is recorded as PAFAH1B1[6].
- lissencephaly due to LIS1 mutation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_95232[7].
- lissencephaly due to LIS1 mutation's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99796[8].
- lissencephaly due to LIS1 mutation's UMLS CUI is recorded as CL939321[9].
- lissencephaly due to LIS1 mutation's ICD-10-CM is recorded as Q04.3[10].
- lissencephaly due to LIS1 mutation's GARD rare disease ID is recorded as 5049[11].
- lissencephaly due to LIS1 mutation's Mondo ID is recorded as MONDO_0011830[12].
- lissencephaly due to LIS1 mutation's ICD-11 ID is recorded as 225516542[13].