Noonan syndrome
ORPHA:648Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculocerebrocutaneous syndrome
ORPHA:1647Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 3
ORPHA:2752Orofaciodigital syndrome type 7
ORPHA:90649Osteogenesis imperfecta type 1
ORPHA:216796Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Painful legs and moving toes syndrome
ORPHA:617440PASS syndrome
ORPHA:641385PEHO syndrome
ORPHA:2836Perlman syndrome
ORPHA:2849POEMS syndrome
ORPHA:2905Primary biliary cholangitis
ORPHA:186Progressive supranuclear palsy
ORPHA:683Recombinant 8 syndrome
ORPHA:96167Ring chromosome 1 syndrome
ORPHA:1437Ring chromosome 11 syndrome
ORPHA:96175Ring chromosome 4 syndrome
ORPHA:1447Ring chromosome 8 syndrome
ORPHA:1450RNU4-2-related autosomal dominant neurodevelopmental disorder
ORPHA:686488Roifman syndrome
ORPHA:353298Sanjad-Sakati syndrome
ORPHA:2323Scimitar syndrome
ORPHA:185Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Severe dermatitis-multiple allergies-metabolic wasting syndrome
ORPHA:369992Severe oculo-renal-cerebellar syndrome
ORPHA:2715Sheehan syndrome
ORPHA:91355Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
ORPHA:397623Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
ORPHA:314394Short stature-optic atrophy-Pelger-Huët anomaly syndrome
ORPHA:391677SHORT syndrome
ORPHA:3163Shwachman-Diamond syndrome
ORPHA:811Smith-Lemli-Opitz syndrome
ORPHA:818Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
ORPHA:521390Structural heart defects-renal anomalies syndrome
ORPHA:689822Sweet syndrome
ORPHA:3243Symphalangism with multiple anomalies of hands and feet
ORPHA:3246Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Thrombocytopenia-absent radius syndrome
ORPHA:3320Thymoma-hypogammaglobulinemia syndrome
ORPHA:169105Tibial aplasia-ectrodactyly syndrome
ORPHA:3329Tricho-dento-osseous syndrome
ORPHA:3352