Phenotypes for disease #00042 (MTDPS3 (mitochondrial DNA depletion syndrome (hepatocerebral), type 3 (MTDPS-3)), OMIM:251880)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000003241 - Unknown - - - - - - - Carl Fratter 00004534
0000003242 - Unknown - - - - - - - Carl Fratter 00004535
0000060600 - Familial, autosomal recessive - - - - - m DNA depletion syndrome 3 (hepatocerebral type) (OMIM:251880) - Daniel Trujillano 00081031
0000060628 - Familial, autosomal recessive - - - - - m DNA depletion syndrome 3 (hepatocerebral type) (OMIM:251880) - Daniel Trujillano 00081059
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