GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095GRACILE syndrome
ORPHA:53693H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Helsmoortel-Van der Aa syndrome
ORPHA:404448Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome
ORPHA:1495Iridocorneal endothelial syndrome
ORPHA:64734Isolated Joubert syndrome
ORPHA:475JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454Joubert syndrome with oculorenal defect
ORPHA:2318KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378Lethal ataxia with deafness and optic atrophy
ORPHA:1187Liddle syndrome
ORPHA:526LIG4 syndrome
ORPHA:99812Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Mohr-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:71211