Phenotypes for disease #01901 (MGCPH (macrocephaly/megalencephaly syndrome, autosomal recessive (MGCPH)), OMIM:248000)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000066578 macrocephaly - - Familial, autosomal dominant - 22.3y - - - Michel van Geel 00086977
0000066612 macrocephaly, keratocyst - - Unknown - 14.9y - - - Michel van Geel 00087011
0000066653 keratocysts, macrocrany, mental retardation - - Unknown - 6.7y - - - Michel van Geel 00087052
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