Laryngeal abductor paralysis
ORPHA:2808Laryngo-onycho-cutaneous syndrome
ORPHA:2407Leukocyte adhesion deficiency type II
ORPHA:99843Linear nevus sebaceus syndrome
ORPHA:2612Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Meacham syndrome
ORPHA:3097Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Mixed connective tissue disease
ORPHA:809Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Multiple benign circumferential skin creases on limbs
ORPHA:2505Multiple 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:623Nelson syndrome
ORPHA:199244Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome with multiple lentigines
ORPHA:500Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234Ocular anomalies-axonal neuropathy-developmental delay syndrome
ORPHA:496790Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Osteosclerotic bone dysplasia
ORPHA:1832Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993Pearson syndrome
ORPHA:699Pierson syndrome
ORPHA:2670POEMS syndrome
ORPHA:2905Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Posterior cortical atrophy
ORPHA:54247Progressive hemifacial atrophy
ORPHA:1214Progressive supranuclear palsy
ORPHA:683Proximal myotonic myopathy
ORPHA:606Pseudoleprechaunism syndrome, Patterson type
ORPHA:2976Ramon syndrome
ORPHA:3019