Netherton syndrome
ORPHA:634Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome
ORPHA:648Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Ocular anomalies-axonal neuropathy-developmental delay syndrome
ORPHA:496790Oculodentodigital dysplasia
ORPHA:2710Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751Orofaciodigital syndrome type 3
ORPHA:2752Orofaciodigital syndrome type 7
ORPHA:90649Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Perlman syndrome
ORPHA:2849PMP22-RAI1 contiguous gene duplication syndrome
ORPHA:477817POEMS syndrome
ORPHA:2905Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Port-wine nevi-mega cisterna magna-hydrocephalus syndrome
ORPHA:2703Primary 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:91355Sheldon-Hall syndrome
ORPHA:1147Short 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:521390Structural heart defects-renal anomalies syndrome
ORPHA:689822Symphalangism with multiple anomalies of hands and feet
ORPHA:3246Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Thrombocytopenia-absent radius syndrome
ORPHA:3320Tricho-dento-osseous syndrome
ORPHA:3352