Phenotypes for disease #03554 (OCCM (cortical malformations, occipital), OMIM:614115)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000085635 Cortical malformation; occipital pachygyria - - Familial, autosomal recessive 33y - - - - Johan den Dunnen 00107881
0000085636 Cortical malformation; occipital pachygyria - - Familial, autosomal recessive 14y - - - - Johan den Dunnen 00107882
0000085637 Cortical malformation; occipital pachygyria - - Familial, autosomal recessive 16y - - - - Johan den Dunnen 00107883
0000268965 HP:0001263; HP:0001999; HP:0001249; HP:0002098; HP:0001252; HP:0000954; HP:0001655; HP:0008081; HP:0000316 - Cortical malformations, occipital (OMIM 614115) Familial, autosomal recessive - - - - - Wenjuan Qiu 00373741
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