Phenotypes for disease #06276 (NEDMEHM (Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination), OMIM:618367)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000326366 - - - Familial, autosomal recessive - - - - Min Peng 00436186
0000326367 - - - Familial, autosomal recessive - - - - Min Peng 00436187
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