Loading disease data
| Disease | Prevalence | Drugs | Proteins | |
|---|---|---|---|---|
| Psoriatic arthritis (PSORAS) | N/A | 59 | 2 | |
| Rheumatoid arthritis (RA) | Uncommon | 402 | 2 | |
| Acrodysostosis 1, with or without hormone resistance (ACRDYS1) | N/A | — | 1 | |
| Acromesomelic dysplasia 4 (AMD4) | N/A | — | 1 | |
| Antley-Bixler syndrome, with genital anomalies and disordered steroidogenesis (ABS1) | N/A | — | 1 | |
| Arthrogryposis, distal, 11 (DA11) | N/A | — | 1 | |
| Autoinflammatory disease, systemic, with vasculitis (SAIDV) | N/A | — | 1 | |
| Autoinflammatory disease, systemic, X-linked (SAIDX) | N/A | — | 1 | |
| Bent bone dysplasia syndrome 2 (BBDS2) | N/A | — | 1 | |
| Brachydactyly B1 (BDB1) | Ultra-Rare | — | 1 | |
| Brachydactyly B2 (BDB2) | Ultra-Rare | — | 1 | |
| C syndrome (CSYN) | Very Rare | — | 1 | |
| Camurati-Engelmann disease 2 (CAEND2) | N/A | — | 1 | |
| Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia (CDP-PBHM) | Ultra-Rare | — | 1 | |
| Congenital myopathy 4A, autosomal dominant (CMYO4A) | N/A | — | 1 | |
| Endocrine-cerebroosteodysplasia (ECO) | Ultra-Rare | — | 1 | |
| Hyaline fibromatosis syndrome (HFS) | Ultra-Rare | — | 1 | |
| Hypophosphatemic rickets, autosomal recessive, 1 (ARHR1) | N/A | — | 1 | |
| Hypophosphatemic rickets, autosomal recessive, 2 (ARHR2) | N/A | — | 1 | |
| Intervertebral disc disease (IDD) | N/A | 5 | 1 | |
| Lacrimo-auriculo-dento-digital syndrome 3 (LADD3) | Ultra-Rare | — | 1 | |
| Metacarpal 4-5 fusion (MF4) | N/A | — | 1 | |
| Metaphyseal anadysplasia 2 (MANDP2) | Ultra-Rare | — | 1 | |
| Multicentric osteolysis, nodulosis, and arthropathy (MONA) | N/A | — | 1 | |
| Multiple epiphyseal dysplasia 1 (EDM1) | N/A | — | 1 | |
| Multiple epiphyseal dysplasia 6 (EDM6) | Ultra-Rare | — | 1 | |
| Multiple synostoses syndrome 1 (SYNS1) | Ultra-Rare | — | 1 | |
| Multiple synostoses syndrome 3 (SYNS3) | Ultra-Rare | — | 1 | |
| Myopathy, centronuclear, 6, with fiber-type disproportion (CNM6) | N/A | — | 1 | |
| Opsismodysplasia (OPSMD) | Ultra-Rare | — | 1 | |
| Orofacial cleft 8 (OFC8) | Uncommon | — | 1 | |
| Osteofibrous dysplasia (OSFD) | N/A | — | 1 | |
| Osteogenesis imperfecta 22 (OI22) | Uncommon | — | 1 | |
| Osteogenesis imperfecta 6 (OI6) | Uncommon | 14 | 1 | |
| Paget disease of bone 5, juvenile-onset (PDB5) | Ultra-Rare | — | 1 | |
| Periodontititis, aggressive, 1 (AP1) | N/A | 1 | 1 | |
| Pseudoachondroplasia (PSACH) | Rare | 1 | 1 | |
| Pyle disease (PYL) | Ultra-Rare | — | 1 | |
| Raine syndrome (RNS) | Ultra-Rare | — | 1 | |
| Rheumatoid arthritis systemic juvenile (RASJ) | Rare | 46 | 1 | |
| Rickets vitamin D-dependent 2A (VDDR2A) | N/A | — | 1 | |
| Robinow syndrome, autosomal recessive 1 (RRS1) | Ultra-Rare | — | 1 | |
| Split-foot malformation with mesoaxial polydactyly (SFMMP) | Ultra-Rare | — | 1 | |
| Split-hand/foot malformation 4 (SHFM4) | Rare | — | 1 | |
| Spondylometaphyseal dysplasia, Pagnamenta type (SMDP) | N/A | — | 1 | |
| Stapes ankylosis with broad thumb and toes (SABTS) | Ultra-Rare | — | 1 | |
| Symphalangism, proximal 1A (SYM1A) | N/A | — | 1 | |
| Tarsal-carpal coalition syndrome (TCC) | Ultra-Rare | — | 1 | |
| Tatton-Brown-Rahman syndrome (TBRS) | Ultra-Rare | — | 1 | |
| Tetraamelia syndrome 2 (TETAMS2) | Ultra-Rare | — | 1 |