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Diseases / Disorder of development or morphogenesis/ Lissencephaly spectrum disorders

Lissencephaly type 3

rare

Identifiers: MONDO:0015148 Orphanet:102011
Part of: Lissencephaly spectrum disorders

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Neu-Laxova syndrome MONDO:0000179 3
Lissencephaly due to TUBA1A mutation MONDO:0012703 TUBA1A
Lissencephaly type 3-familial fetal akinesia sequence syndrome MONDO:0019449
Lissencephaly type 3-metacarpal bone dysplasia syndrome MONDO:0011004

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