Pendred syndrome
ORPHA:705PENS syndrome
ORPHA:313936Perlman syndrome
ORPHA:2849Perry syndrome
ORPHA:178509PFAPA syndrome
ORPHA:42642PHACE syndrome
ORPHA:42775PHAVER syndrome
ORPHA:2876PIBIDS syndrome
ORPHA:670Pierson syndrome
ORPHA:2670PMM2-CDG
ORPHA:79318POEMS syndrome
ORPHA:2905Poland syndrome
ORPHA:2911Pollitt syndrome
ORPHA:75790Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome
ORPHA:500533Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Progeroid syndrome, Petty type
ORPHA:2963Progressive supranuclear palsy
ORPHA:683Proteasome-associated autoinflammatory syndrome
ORPHA:324977Proteus syndrome
ORPHA:744PsAPASH syndrome
ORPHA:641390Pseudopseudohypoparathyroidism
ORPHA:79445Pudendal nerve entrapment syndrome
ORPHA:60039PUM1-associated developmental disability-ataxia-seizure syndrome
ORPHA:589515Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
ORPHA:71289Right isomerism
ORPHA:97548Ring chromosome 1 syndrome
ORPHA:1437Ring chromosome 4 syndrome
ORPHA:1447Ring chromosome 8 syndrome
ORPHA:1450Sanjad-Sakati syndrome
ORPHA:2323SAPHO syndrome
ORPHA:793Seizures-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:391677Smith-Lemli-Opitz syndrome
ORPHA:818Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
ORPHA:521390Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Tetraamelia-multiple malformations syndrome
ORPHA:3301Thrombocytopenia-absent radius syndrome
ORPHA:3320Tricho-dento-osseous syndrome
ORPHA:3352Triphalangeal thumb-polysyndactyly syndrome
ORPHA:2950Triple A syndrome
ORPHA:869Trisomy 13 syndrome
ORPHA:3378Trisomy X syndrome
ORPHA:3375Van der Woude syndrome
ORPHA:888