Phenotypes for disease #03932 (CDCBM4 (dysplasia ,cortical, complex, with other brain malformations, type 4 (CDCBM-4)), OMIM:615412)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000106789 Pachygyria over the posterior frontal lobe and parieto-occipital cortex - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134040
0000106790 Agyria, diffuse - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134041
0000106791 Pachygyria diffuse, mild over frontal lobes, moderate posterior - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134042
0000106792 Pachygyria diffuse, cell sparse zone over occipital lobes - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134043
0000106793 Pachygyria diffuse, mild over frontal lobe and moderate over temporal and occipital lobes - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134044
0000106794 Pachygyria, diffuse, mild over frontal lobe and moderate over temporal and occipital lobes - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134045
0000106795 Pachygyria, nearly normal cortex over frontal lobes, pachygyria over perisylvian and occipital lobes - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134046
0000106796 Pachygyria diffuse, mild over frontal lobe, moderate over temporal > occipital lobes, bilateral deep - - Familial, autosomal dominant - - - - - Katrien Stouffs 00134047
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