Proximal myotonic myopathy
ORPHA:606Prune belly syndrome
ORPHA:2970Recombinant 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:686488Rudiger syndrome
ORPHA:3118Sagliker syndrome
ORPHA:300493Sandifer syndrome
ORPHA:71272Sanjad-Sakati syndrome
ORPHA:2323Seckel syndrome
ORPHA:808Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Serpentine fibula-polycystic kidneys syndrome
ORPHA:2853Severe 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:818Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
ORPHA:521390Stickler syndrome
ORPHA:828Stimmler syndrome
ORPHA:3199Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952TAFRO syndrome
ORPHA:457077TARP syndrome
ORPHA:2886TEMPI syndrome
ORPHA:284227Temple syndrome
ORPHA:254516Temtamy syndrome
ORPHA:1777Thomas syndrome
ORPHA:3316Thrombocytopenia-absent radius syndrome
ORPHA:3320Tietz syndrome
ORPHA:42665Timothy syndrome
ORPHA:65283Townes-Brocks syndrome
ORPHA:857Tremor-ataxia-central hypomyelination syndrome
ORPHA:447896Tricho-dento-osseous syndrome
ORPHA:3352Trichodental syndrome
ORPHA:3351Triphalangeal thumb-polysyndactyly syndrome
ORPHA:2950Triple A syndrome
ORPHA:869Trisomy X syndrome
ORPHA:3375Tubulointerstitial nephritis and uveitis syndrome
ORPHA:91500Tumor necrosis factor receptor 1 associated periodic syndrome
ORPHA:32960Turner syndrome
ORPHA:881Usher syndrome
ORPHA:886VIPoma
ORPHA:97282