Laurin-Sandrow syndrome
ORPHA:2378Lethal ataxia with deafness and optic atrophy
ORPHA:1187LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Mixed connective tissue disease
ORPHA:809Mohr-Tranebjaerg syndrome
ORPHA:52368MOMO syndrome
ORPHA:2563Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112MORM syndrome
ORPHA:75858Mosaic trisomy 8 syndrome
ORPHA:96061MRCS syndrome
ORPHA:263347Multiple 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:623NARP syndrome
ORPHA:644Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234Oculocerebrorenal syndrome of Lowe
ORPHA:534Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Omenn syndrome
ORPHA:39041Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Painful legs and moving toes syndrome
ORPHA:617440PARC syndrome
ORPHA:2825