EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Feingold syndrome
ORPHA:1305Fibrous dysplasia/McCune-Albright syndrome
ORPHA:595216Fragile X syndrome
ORPHA:908Fragile X-associated tremor/ataxia syndrome
ORPHA:93256Glossopalatine ankylosis
ORPHA:141163GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Growth deficiency-brachydactyly-dysmorphism syndrome
ORPHA:2055H syndrome
ORPHA:168569Hajdu-Cheney syndrome
ORPHA:955HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Holmes-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:2268Indolent primary cutaneous T-cell lymphoma
ORPHA:178548Intellectual 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:79403KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal omphalocele-cleft palate syndrome
ORPHA:2736LIG4 syndrome
ORPHA:99812Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466May-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:2556Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112