All diseases

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06163 CODA Cavitary optic disc anomalies 611543 AD - - MMP19 - -
02618 COPD pulmonary disease, obstructive, chronic, susceptibility to (COPD) 606963 - 8 3 HMOX1, MMP1, SERPINA1 - -
00331 MANDP1 anadysplasia, metaphyseal, type 1 (MANDP-1, dysplasia, spondyloepimetaphyseal, Missouri type) 602111 AD 5 5 MMP13 - -
05178 MDST dysplasia, metaphyseal, Spahr type (MDST) 250400 AR 1 1 MMP13 - -
01773 RDEB epidermolysis bullosa dystrophica, autosomal recessive (RDEB) 226600 AR 418 411 COL7A1, MMP1 - -
04581 WNCHRS Winchester? syndrome (WNCHRS) 277950 - 2 2 MMP14 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.