PASS syndrome
ORPHA:641385PEHO syndrome
ORPHA:2836PEHO-like syndrome
ORPHA:99807Pentasomy X syndrome
ORPHA:11POEMS syndrome
ORPHA:2905Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome
ORPHA:500533Port-wine nevi-mega cisterna magna-hydrocephalus syndrome
ORPHA:2703Progressive supranuclear palsy
ORPHA:683Proteasome-associated autoinflammatory syndrome
ORPHA:324977Rett syndrome
ORPHA:778Ring 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:686488Sanjad-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 stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome
ORPHA:589442SHORT 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:689822Sweet syndrome
ORPHA:3243Symphalangism with multiple anomalies of hands and feet
ORPHA:3246Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952TARP syndrome
ORPHA:2886Tetrasomy X syndrome
ORPHA:9Thrombocytopenia-absent radius syndrome
ORPHA:3320Thymoma-hypogammaglobulinemia syndrome
ORPHA:169105Tibial aplasia-ectrodactyly syndrome
ORPHA:3329Toxic epidermal necrolysis
ORPHA:537Tricho-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:881Van der Woude syndrome
ORPHA:888VIPoma
ORPHA:97282