All diseases

8 entries on 1 page. Showing entries 1 - 8.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00650 - Jackson-Weiss syndrome 123150 - - - FGFR1, FGFR2 - -
04474 FGFR-1OP myeloproliferative disorder (FGFR-1OP) 605392 - - - FGFR1OP - -
00651 HH-2 hypogonadism, hypogonadotropic, type 2 with/without anosmia (HH-2) 147950 - - - FGFR1 - -
04473 HRTFDS Hartsfield syndrome (HRTFDS) 615465 - - - FGFR1 - -
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 - -
00652 OGD dysplasia, osteoglophonic (OGD) 166250 - - - FGFR1 - -
00526 Pfeiffer Pfeiffer syndrome 101600 - - - FGFR1, FGFR2 - -
00653 TRIGNO-1 trigonocephaly, type 1 (TRIGNO-1) 190440 - - - FGFR1 - -
Legend   How to query