Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Mohr-Tranebjaerg syndrome
ORPHA:52368MOMO syndrome
ORPHA:2563Monosomy 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:69087Nail-patella-like renal disease
ORPHA:2613NAME syndrome
ORPHA:623Nelson syndrome
ORPHA:199244Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome
ORPHA:453499Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234Oculodentodigital dysplasia
ORPHA:2710Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Okamoto syndrome
ORPHA:2729Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183OSLAM syndrome
ORPHA:2760Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Painful legs and moving toes syndrome
ORPHA:617440PARC syndrome
ORPHA:2825PASS syndrome
ORPHA:641385Pearson syndrome
ORPHA:699PEHO syndrome
ORPHA:2836Pierson syndrome
ORPHA:2670POEMS syndrome
ORPHA:2905Port-wine nevi-mega cisterna magna-hydrocephalus syndrome
ORPHA:2703Posterior cortical atrophy
ORPHA:54247Primary progressive aphasia
ORPHA:95432Progressive supranuclear palsy
ORPHA:683Proteasome-associated autoinflammatory syndrome
ORPHA:324977