LUMBAR syndrome
ORPHA:83628Matthew-Wood syndrome
ORPHA:2470Mesomelia-synostoses syndrome
ORPHA:2496Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 9p syndrome
ORPHA:261112Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Musculocontractural Ehlers-Danlos syndrome
ORPHA:2953Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841N syndrome
ORPHA:2608Neuromyelitis 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:592869Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183PAGOD 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:641385Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome
ORPHA:444138PEHO syndrome
ORPHA:2836Pendred syndrome
ORPHA:705PENS syndrome
ORPHA:313936Perry syndrome
ORPHA:178509PFAPA syndrome
ORPHA:42642PHACE syndrome
ORPHA:42775PHAVER syndrome
ORPHA:2876PIBIDS syndrome
ORPHA:670POEMS syndrome
ORPHA:2905Poland syndrome
ORPHA:2911Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome
ORPHA:500533Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
ORPHA:171848Progeroid syndrome, Petty type
ORPHA:2963Progressive supranuclear palsy
ORPHA:683Pseudohypoparathyroidism type 1A
ORPHA:79443PUM1-associated developmental disability-ataxia-seizure syndrome
ORPHA:589515Roberts syndrome
ORPHA:3103SAPHO syndrome
ORPHA:793Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Severe dermatitis-multiple allergies-metabolic wasting syndrome
ORPHA:369992Tetraamelia-multiple malformations syndrome
ORPHA:3301Triphalangeal thumb-polysyndactyly syndrome
ORPHA:2950