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Showing below up to 50 results in range #24,451 to #24,500.
- Fetus or newborn affected by amnionitis (Q88359)
- Effective registration for organ transplantation with high urgency status (Q88358)
- CHST3-related skeletal dysplasia (Q88357)
- Spondyloepimetaphyseal dysplasia, Bieganski type (Q88356)
- Spondyloepimetaphyseal dysplasia, X-linked (Q88355)
- Spondyloenchondrodysplasia (Q88354)
- Spondyloepimetaphyseal dysplasia - abnormal dentition (Q88353)
- Spondyloepimetaphyseal dysplasia - multiple dislocations (Q88352)
- Spondyloepimetaphyseal dysplasia, Missouri type (Q88351)
- Spondyloepimetaphyseal dysplasia, Genevieve type (Q88350)
- Spondyloepimetaphyseal dysplasia, aggrecan type (Q88349)
- Spondyloepimetaphyseal dysplasia, Shohat type (Q88348)
- Spondyloepiphyseal dysplasia, Byers type (Q88347)
- Spondyloepimetaphyseal dysplasia, Irapa type (Q88346)
- Smith-McCort dysplasia (Q88345)
- Spondyloepiphyseal dysplasia, Reardon type (Q88344)
- Spondyloepiphyseal dysplasia, Cantu type (Q88343)
- Spondyloepiphyseal dysplasia, Omani type (Q88342)
- Spondylar and nasal alterations with striated metaphyses dysplasia (Q88341)
- Spondyloepiphyseal dysplasia, Pakistani type (Q88340)
- Spondyloepimetaphyseal dysplasia - joint laxity (Q88339)
- Spondyloepiphyseal dysplasia, Nishimura type (Q88338)
- Dyggve-Melchior-Clausen disease (Q88337)
- Spondyloepimetaphyseal dysplasia, matrilin-3 type (Q88336)
- Metatropic dysplasias (Q88335)
- Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Q88334)
- Spondyloepiphyseal dysplasia, Maroteaux type (Q88333)
- Dyssegmental dysplasia, Silverman-Handmaker type (Q88332)
- Spondyloepiphyseal dysplasia, Kimberley type (Q88331)
- Spondyloepiphyseal dysplasia tarda, Kohn type (Q88330)
- Spondyloepiphyseal dysplasia tarda, X-linked (Q88329)
- Otospondylomegaepiphyseal dysplasia (Q88328)
- Schneckenbecken dysplasia (Q88327)
- Weissenbacher- Zweymuller syndrome (Q88326)
- Fibrochondrogenesis (Q88325)
- Dyssegmental dysplasia, Rolland-Desbuquois type (Q88324)
- Spondyloperipheral dysplasia - short ulna (Q88323)
- Wassermann's test (Q88322)
- Czech dysplasia, metatarsal type (Q88321)
- Congenital spondyloepiphyseal dysplasia (Q88320)
- Traumatic subluxation of joint (Q88319)
- Sequelae of dislocation of unspecified body region (Q88318)
- Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis (Q88317)
- Interstitial myositis, ankle or foot (Q88316)
- Special screening examination for chlamydial diseases (Q88315)
- Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Q88314)
- Kniest dysplasia (Q88313)
- Interstitial myositis, head (Q88312)
- Interstitial myositis, upper arm (Q88311)
- Interstitial myositis, neck (Q88310)
