Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Liddle syndrome
ORPHA:526LIG4 syndrome
ORPHA:99812Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
ORPHA:457485Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Maxillonasal dysplasia
ORPHA:1248Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Miller Fisher syndrome
ORPHA:98919MOMO syndrome
ORPHA:2563Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mucopolysaccharidosis type 2
ORPHA:580Multiple 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:245Nail-patella syndrome
ORPHA:2614NAME syndrome
ORPHA:623Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717Odontomatosis-aortae esophagus stenosis syndrome
ORPHA:2724Oley syndrome
ORPHA:79458Oliver syndrome
ORPHA:2920Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993PEHO syndrome
ORPHA:2836