Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome
ORPHA:313800Rett syndrome
ORPHA:778Revesz syndrome
ORPHA:3088Reye syndrome
ORPHA:3096Rh deficiency syndrome
ORPHA:71275RHYNS syndrome
ORPHA:140976RIDDLE syndrome
ORPHA:420741RIN2 syndrome
ORPHA:217335Ring chromosome 1 syndrome
ORPHA:1437Ring chromosome 22 syndrome
ORPHA:1446Ring chromosome 4 syndrome
ORPHA:1447Ring chromosome 8 syndrome
ORPHA:1450RNU4-2-related autosomal dominant neurodevelopmental disorder
ORPHA:686488Roberts syndrome
ORPHA:3103Robinow syndrome
ORPHA:97360Roifman syndrome
ORPHA:353298Rombo syndrome
ORPHA:3110Rotor syndrome
ORPHA:3111Rowell syndrome
ORPHA:658584Rudiger syndrome
ORPHA:3118Sanjad-Sakati syndrome
ORPHA:2323SCALP syndrome
ORPHA:370052SCARF syndrome
ORPHA:3134Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Severe dermatitis-multiple allergies-metabolic wasting syndrome
ORPHA:369992Severe oculo-renal-cerebellar syndrome
ORPHA:2715Short 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:3163Smith-Lemli-Opitz syndrome
ORPHA:818Sotos syndrome
ORPHA:821Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
ORPHA:521390Structural heart defects-renal anomalies syndrome
ORPHA:689822Subaortic stenosis-short stature syndrome
ORPHA:3191Sweet syndrome
ORPHA:3243Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Thiamine-responsive megaloblastic anemia syndrome
ORPHA:49827Thrombocytopenia-absent radius syndrome
ORPHA:3320Thymoma-hypogammaglobulinemia syndrome
ORPHA:169105Townes-Brocks syndrome
ORPHA:857Tricho-dento-osseous syndrome
ORPHA:3352Tricho-retino-dento-digital syndrome
ORPHA:1264Triple A syndrome
ORPHA:869Trisomy X syndrome
ORPHA:3375Tubulointerstitial nephritis and uveitis syndrome
ORPHA:91500Turner syndrome
ORPHA:881