Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841Myhre syndrome
ORPHA:2588N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087NAME syndrome
ORPHA:623Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Noonan syndrome-like disorder with loose anagen hair
ORPHA:2701Oculotrichoanal syndrome
ORPHA:2717Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Painful legs and moving toes syndrome
ORPHA:617440PASS syndrome
ORPHA:641385Perry syndrome
ORPHA:178509POEMS syndrome
ORPHA:2905Port-wine nevi-mega cisterna magna-hydrocephalus syndrome
ORPHA:2703Postaxial acrofacial dysostosis
ORPHA:246Primary cutaneous T-cell lymphoma
ORPHA:171901Primary progressive aphasia
ORPHA:95432Progressive supranuclear palsy
ORPHA:683RIN2 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:686488Rombo syndrome
ORPHA:3110Sanjad-Sakati syndrome
ORPHA:2323SCALP syndrome
ORPHA:370052Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Severe dermatitis-multiple allergies-metabolic wasting syndrome
ORPHA:369992Severe oculo-renal-cerebellar syndrome
ORPHA:2715Sézary syndrome
ORPHA:3162Short 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:521390Sweet syndrome
ORPHA:3243Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Thrombocytopenia-absent radius syndrome
ORPHA:3320Thymoma-hypogammaglobulinemia syndrome
ORPHA:169105Townes-Brocks syndrome
ORPHA:857