MAGIC syndrome
ORPHA:324972Majeed syndrome
ORPHA:77297Malpuech syndrome
ORPHA:2453Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Mandibulofacial dysostosis-microcephaly syndrome
ORPHA:79113Marfan syndrome
ORPHA:558Marshall syndrome
ORPHA:560MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Mazabraud syndrome
ORPHA:57782Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479MEHMO syndrome
ORPHA:85282Meigs syndrome
ORPHA:314451Melorheostosis with osteopoikilosis
ORPHA:1879MEND syndrome
ORPHA:401973MEPAN syndrome
ORPHA:508093Micro syndrome
ORPHA:2510Microcornea-myopic chorioretinal atrophy-telecanthus syndrome
ORPHA:369970Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome
ORPHA:231736Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Mills syndrome
ORPHA:94091MMEP syndrome
ORPHA:3434MOMO syndrome
ORPHA:2563MORM syndrome
ORPHA:75858Mosaic Legius syndrome
ORPHA:634511MRCS syndrome
ORPHA:263347Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
ORPHA:500135Muscle-eye-brain disease
ORPHA:588Myhre syndrome
ORPHA:2588N syndrome
ORPHA:2608Noonan syndrome with multiple lentigines
ORPHA:500Noonan syndrome-like disorder with loose anagen hair
ORPHA:2701Oculocerebrorenal syndrome of Lowe
ORPHA:534Oculotrichoanal syndrome
ORPHA:2717Orofaciodigital syndrome type 2
ORPHA:2751Orofaciodigital syndrome type 4
ORPHA:2753RIN2 syndrome
ORPHA:217335Short rib-polydactyly syndrome, Majewski type
ORPHA:93269Short stature due to growth hormone qualitative anomaly
ORPHA:629Symphalangism with multiple anomalies of hands and feet
ORPHA:3246Toxic epidermal necrolysis
ORPHA:537W syndrome
ORPHA:2804X-linked dystonia-parkinsonism
ORPHA:53351