All diseases

14 entries on 1 page. Showing entries 1 - 14.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00511 - asthma, susceptibility to 600807 AD 1 1 ADRB2, ALOX5, CCL11, HLA-G, HNMT, IL13, MUC7, PHF11, PLA2G7, SCGB3A2, TNF - -
00496 F11D facotr XI deficiency (F11D) 612416 - 57 1 F11 - -
01514 FEO osteolysis, familial expansile (FEO, McCabe disease) 174810 AD - - TNFRSF11A - -
00139 ID intellectual disability (ID) - - 2799 2480 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 556 more - -
01397 IGER IgEresponsiveness, atopic (IGER) 147050 AD - - HAVCR1, IL21R, IL4R, MS4A2, PHF11, PLA2G7, SELP, SPINK5 - autosomal dominant
00010 MCLMR microcephaly with/without chorioretinopathy, lymphedema, or mental retardation (MCLMR) 152950 AD 85 60 KIF11 - -
02954 MODY7 diabetes of the young, maturity-onset, type 7 (MODY-7) 610508 - - - KLF11 - -
05537 OCA albinism, oculocutaneous - - 87 51 C10orf11, SLC24A5 - -
00850 OCA7 albinism, oculocutaneous, type VII (OCA7) 615179 AR - - C10orf11 - -
01992 OPTB2 osteopetrosis, autosomal recessive, type 2 (OPTB-2) 259710 AR - - TNFSF11 - -
03117 OPTB7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 AR 1 - TNFRSF11A - -
02411 PDB2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 AD - - TNFRSF11A - -
01856 PDB5 Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia) 239000 AR - - TNFRSF11B - -
04326 TTD5 trichothiodystrophy, type 5, nonphotosensitive (TTD-5) 300953 XLD 3 1 RNF113A - X-linked dominant
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