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Disease: Lissencephaly
disease
660 words
KG: ent-dise-f7aacf2c
2026-03-21
kind:disease
section:diseases
state:published
Contents
Lissencephaly
Disease Info
DCX (Doublecortin)
X-linked dominant
LIS1 (PAFAH1B1)
Autosomal dominant
ARX
X-linked
TUBA1A
Autosomal dominant
RELN
Autosomal recessive
Databases
OMIM
Orphanet
ClinicalTrials
PubMed
Knowledge Graph
Related Hypotheses (2)
Reelin-Mediated Cytoskeletal Stabilization Protocol
Score: 0.45
Quantum Coherence Disruption in Cellular Communication
Score: 0.34
Related Analyses (4)
Autophagy-lysosome pathway convergence across neurodegenerat
neurodegeneration · archived
Protein aggregation cross-seeding across neurodegenerative d
neurodegeneration · archived
Metabolic reprogramming in neurodegenerative disease
neurodegeneration · completed
Selective vulnerability of entorhinal cortex layer II neuron
neurodegeneration · archived
Related Experiments (3)
PAFAH1B1/LIS1 mutations in type 1 lissencephaly
exploratory · proposed · Score: 0.80
Doublecortin (DCX) mutations in type 1 lissencephaly
exploratory · proposed · Score: 0.80
Reelin pathway defects in human type 2 lissencephaly
exploratory · proposed · Score: 0.70