All diseases

15 entries on 1 page. Showing entries 1 - 15.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00594 - achondroplasia 100800 - - - FGFR3 - -
00595 - Hypochondroplasia 146000 - - - FGFR3 - -
00597 - Crouzon syndrome, with acanthosis nigricans 612247 - - - FGFR3 - -
00598 - cancer, cervical, somatic 603956 - - - FGFR3 - -
00600 - nevus, epidermal 162900 - - - FGFR3, HRAS, NRAS, PIK3CA - -
00602 - Spermatocytic seminoma, somatic 273300 - - - BCL10, FGFR3, KIT, STK11 - -
00315 cancer, bladder cancer, bladder 109800 - - - FGFR3, HRAS, KRAS, RB1 - -
00447 CATSHL camptodactyly, tall stature, hearing loss (CATSHL syndrome) 610474 - - - FGFR3 - -
00091 CRC cancer, colorectal (CRC) 114500 - - - AKT1, APC, AURKA, AXIN2, BAX, BUB1B, CCND1, CTNNB1, DCC, DLC1, EP300, FGFR3, FLCN, MCC, MLH3, NRAS, NTHL1, ODC1, PDGFRL, PIK3CA, 7 more - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
00599 LADD lacrimoauriculodentodigital syndrome ((LADD), Levy-Hollister) 149730 - - - FGF10, FGFR2, FGFR3 - -
00527 MNKES Muenke syndrome (MNKES) 602849 - - - FGFR3 - -
04475 SADDAN SADDAN 616482 - - - FGFR3 - -
00596 TD-1 dysplasia, thanatophoric, type I (TD-1) 187600 - - - FGFR3 - -
00601 TD-2 dysplasia, thanatophoric, type II (TD-2) 187601 - - - FGFR3 - -
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