Phenotypes for disease #01052 (MTDPS1 (mitochondrial DNA depletion syndrome, type 1 (MTDPS-1, MNGIE type)), OMIM:603041)

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     
0000188751 Elevated thymidine, ptosis, PEO, peripheral neuropathy MNGIE MNGIE Familial, autosomal recessive 36y 36y - adolescence Thymidine Phosphorylase Kimberly Kripps 00250187
0000188752 Elevated thymidine, liver cirrhosis and failure, hearing loss Liver failure MNGIE Familial, autosomal recessive - - 00y14m 14m Thymidine Phosphorylase Kimberly Kripps 00250188
0000188753 severe gastrointestinal dysmotility, fatigue, weakness, extremity paresthesias MNGIE MNGIE Familial, autosomal recessive - 20y - - Thymidine Phosphorylase Kimberly Kripps 00250189
0000188754 demyelinating neuropathy, liver cirrhosis, gastric dysmotility - MNGIE Familial, autosomal recessive - 22y - 14y Thymidine Phosphorylase Kimberly Kripps 00250190
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