All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05525 MOPD dwarfism, primordial, osteodysplastic, microcephalic (MOPD) - - 60 60 PCNT, RNU4ATAC - -
01681 MOPD1 dwarfism, primordial, osteodysplastic, microcephalic, type 1 (MOPD-1, Taybi-Linder syndrome) 210710 AR 1 1 RNU4ATAC - -
05393 RFMN Roifman syndrome (RFMN) 616651 AR 5 5 RNU4ATAC - autosomal recessive
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