EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Eng-Strom syndrome
ORPHA:1937Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Fragile X syndrome
ORPHA:908Furlong syndrome
ORPHA:97295Glossopalatine ankylosis
ORPHA:141163GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569Hajdu-Cheney syndrome
ORPHA:955HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome
ORPHA:404473Iridocorneal endothelial syndrome
ORPHA:64734Isolated congenital onychodysplasia
ORPHA:79144JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454Junctional epidermolysis bullosa with pyloric atresia
ORPHA:79403Jung syndrome
ORPHA:2321KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477KLHL7-related Bohring-Opitz-like and Crisponi/Cold-induced sweating-like overlap syndrome
ORPHA:603684L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal omphalocele-cleft palate syndrome
ORPHA:2736Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
ORPHA:457485Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649May-Thurner syndrome
ORPHA:675404Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalocornea-intellectual disability syndrome
ORPHA:2479Microcephaly-capillary malformation syndrome
ORPHA:294016Microphthalmia with linear skin defects syndrome
ORPHA:2556MOMO syndrome
ORPHA:2563Monosomy 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:588