All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01421 - anemia, macrocytic, refractory, due to 5q deletion, somatic 153550 - - - RPS14 - -
06052 COXPD38 ?Combined oxidative phosphorylation deficiency 38 618378 AR - - MRPS14 - -
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