KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngeal abductor paralysis-intellectual disability syndrome
ORPHA:2375Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378Legius syndrome
ORPHA:137605LUMBAR syndrome
ORPHA:83628Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Matthew-Wood syndrome
ORPHA:2470Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Moebius syndrome
ORPHA:570Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 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:588Musculocontractural Ehlers-Danlos syndrome
ORPHA:2953Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087NAME syndrome
ORPHA:623Neuromyelitis optica spectrum disorder
ORPHA:71211Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies
ORPHA:592850Neuromyelitis optica spectrum disorder with anti-MOG antibodies
ORPHA:592856Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies
ORPHA:592869Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234OBSOLETE: Oculocerebroosseous syndrome
ORPHA:2708Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751Otofaciocervical syndrome
ORPHA:2792PAGOD syndrome
ORPHA:991Pai syndrome
ORPHA:1993Painful legs and moving toes syndrome
ORPHA:617440PAPA syndrome
ORPHA:69126PAPASH syndrome
ORPHA:641380PARC syndrome
ORPHA:2825PASH syndrome
ORPHA:289478PASS syndrome
ORPHA:641385