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
03160 ALS11 sclerosis, lateral, amyotrophic, type type 11 (ALS11) 612577 AD 1 1 FIG4 - -
04477 BTOP polymicrogyria?, bilateral temporooccipital (BTOP) 612691 AR - - FIG4 - -
03016 CMT4J Charcot-Marie-Tooth disease, type 4J (CMT-4J) 611228 AR 6 7 FIG4 - -
01714 YVS Yunis Varon syndrome (YVS) 216340 AR 1 1 FIG4 - -
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