All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00904 ALSG aplasia of lacrimal and salivary glands (ALSG) 180920 AD 5 5 FGF10 - -
07088 DEE90 encephalopathy, developmental and epileptic, type 90 301058 XLD;XLR - - FGF13 - -
06571 EIEE47 Epileptic encephalopathy, early infantile, 47 617166 AD - - FGF12 - -
03874 HH20 hypogonadism, hypogonadotropic, type 20 with/without anosmia (HH-20) 615270 AD - - FGF17 - -
00599 LADD lacrimoauriculodentodigital syndrome - AD 9 9 FGF10, FGFR2, FGFR3 - -
07090 LADD3 lacrimoauriculodentodigital syndrome, type 3 620193 AD - - FGF10 - -
06875 MF4 Metacarpal 4-5 fusion 309630 XLR - - FGF16 - -
04167 SCA ataxia, spinocerebellar (SCA) - - 194 189 FGF14, NOP56, NPTX1 - -
02844 SCA27A ataxia, spinocerebellar, type 27A 193003 AD 1 - FGF14 - -
07066 SCA27B ataxia, spinocerebellar, type 27B 620174 AD - - FGF14 - -
07089 XLID110 intellectual developmental disorder, X-linked type 110 301095 XLR - - FGF13 - -
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