All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00050 hydrops fetalis hydrops fetalis - - 9 8 ANGPT2 - -
05780 LMPHM lymphatic malformation (LMPHM) - - 6 6 ANGPT2 - -
06903 LMPHM10 lymphatic malformation, type 10 619369 AD - - ANGPT2 - -
04492 MRT49 mental retardation?, autosomal recessive, type 49 (MRT-49) 616281 AR - - GPT2 - -
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