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MCID: LSS023
MIFTS: 5
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Lissencephaly with Cerebellar Hypoplasia Type C
Categories:
Fetal diseases, Genetic diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Lissencephaly with Cerebellar Hypoplasia Type C:
Name: Lissencephaly with Cerebellar Hypoplasia Type C
58
Classifications:
MalaCards categories:
Global: Fetal diseases Rare diseases Genetic diseases Anatomical: Neuronal diseases
ICD10:
33
Orphanet: 58
Rare neurological diseases
Developmental anomalies during embryogenesis External Ids:
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MalaCards based summary :
Lissencephaly with Cerebellar Hypoplasia Type C Affiliated tissues include brain.
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MalaCards organs/tissues related to Lissencephaly with Cerebellar Hypoplasia Type C:40
Brain
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Search
GEO
for disease gene expression data for Lissencephaly with Cerebellar Hypoplasia Type C.
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