Laryngo-onycho-cutaneous syndrome
ORPHA:2407Léri-Weill dyschondrosteosis
ORPHA:240Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Marden-Walker syndrome
ORPHA:2461Maxillonasal dysplasia
ORPHA:1248Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Miller Fisher syndrome
ORPHA:98919Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mosaic trisomy 8 syndrome
ORPHA:96061Mucopolysaccharidosis type 2
ORPHA:580Mueller-Weiss syndrome
ORPHA:566943Multiple endocrine neoplasia type 1
ORPHA:652Multiple 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:69087Nager syndrome
ORPHA:245NAME syndrome
ORPHA:623NARP syndrome
ORPHA:644Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculocerebrorenal syndrome of Lowe
ORPHA:534Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Odontomatosis-aortae esophagus stenosis syndrome
ORPHA:2724Oliver syndrome
ORPHA:2920Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 7
ORPHA:90649Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Parkes Weber syndrome
ORPHA:90307PHAVER syndrome
ORPHA:2876POEMS syndrome
ORPHA:2905Postaxial acrofacial dysostosis
ORPHA:246Progressive supranuclear palsy
ORPHA:683Proximal myotonic myopathy
ORPHA:606Ptosis-vocal cord paralysis syndrome
ORPHA:2997Recombinant 8 syndrome
ORPHA:96167