Phenotypes for disease #00623 (MEGDEL (3-methylglutaconic aciduria with deafness, encephalopathy, Leigh-like syndrome (MEGDEL)), OMIM:614739)

16 entries on 1 page. Showing entries 1 - 16.
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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     
0000060518 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome (OMIM:614739) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080949
0000079137 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100918
0000079138 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100919
0000079139 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100920
0000079140 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100921
0000079141 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100922
0000079142 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100923
0000079143 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100924
0000079144 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100925
0000079145 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100926
0000079146 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100927
0000079147 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100928
0000079148 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100929
0000079149 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100930
0000079150 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100931
0000079151 see paper; … - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100932
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