All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00645 ACHP acheiropody (ACHP) 200500 AR 5 5 LMBR1 - -
04558 LSS Laurin-Sandrow syndrome (LSS) 135750 AD - - LMBR1 - -
00646 PPD2 polydactyly, preaxial, type II (PPD-2) 174500 AD 2 2 LMBR1 - autosomal dominant
00647 SDTY4 syndactyly, type IV (SDTY-4) 186200 AD - - LMBR1 - -
04557 THYP tibia, hypoplastic or aplastic, with polydactyly (THYP) 188740 AD - - LMBR1 - -
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