Phenotypes for disease #05376 (NDMSCA (neurodevelopmental disorder with microcephaly, seizures, cortical atrophy (NDMSCA)), OMIM:617802)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000257302 - - Global developmental delay, seizures, spasticity, microcephaly Familial, autosomal recessive - - - - Anju Shukla 00361906
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