Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087NAME syndrome
ORPHA:623Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculodental syndrome, Rutherfurd type
ORPHA:2709Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Osteosclerotic bone dysplasia
ORPHA:1832Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993POEMS syndrome
ORPHA:2905Progressive hemifacial atrophy
ORPHA:1214Progressive supranuclear palsy
ORPHA:683Proteasome-associated autoinflammatory syndrome
ORPHA:324977Proximal myotonic myopathy
ORPHA:606Pudendal nerve entrapment syndrome
ORPHA:60039Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
ORPHA:71289Ramon syndrome
ORPHA:3019Ravine syndrome
ORPHA:99852Recombinant 8 syndrome
ORPHA:96167Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome
ORPHA:313800Rett syndrome
ORPHA:778Revesz syndrome
ORPHA:3088Reye syndrome
ORPHA:3096Rh deficiency syndrome
ORPHA:71275RHYNS syndrome
ORPHA:140976RIDDLE syndrome
ORPHA:420741RIN2 syndrome
ORPHA:217335Ring chromosome 1 syndrome
ORPHA:1437Ring chromosome 11 syndrome
ORPHA:96175Ring chromosome 22 syndrome
ORPHA:1446Ring chromosome 4 syndrome
ORPHA:1447Ring chromosome 8 syndrome
ORPHA:1450RNU4-2-related autosomal dominant neurodevelopmental disorder
ORPHA:686488Roberts syndrome
ORPHA:3103Robinow syndrome
ORPHA:97360Roifman syndrome
ORPHA:353298Rombo syndrome
ORPHA:3110