Phenotypes for disease #03181 (MCPH7 (microcephaly, type 7, autosomal recessive (MCPH-7)), OMIM:612703)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

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Age/Diagnosis     

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Owner     

Individual ID     
0000068432 prenatal microcephaly with simplified gyral pattern, partial agenesis of corpus callosum, pachygyria - - Familial, autosomal recessive - prenatal - - - Francesca Cristofoli 00089033
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