HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hereditary hyperekplexia
ORPHA:3197Hereditary persistence of fetal hemoglobin-intellectual disability syndrome
ORPHA:619233Hyperornithinemia-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-early-onset cataract-microcephaly syndrome
ORPHA:633035Intellectual disability-spasticity-ectrodactyly syndrome
ORPHA:1891Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
ORPHA:2698L1 syndrome
ORPHA:275543Lacrimoauriculodentodigital syndrome
ORPHA:2363Lambert syndrome
ORPHA:1296Laron syndrome
ORPHA:633Larsen syndrome
ORPHA:503Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lateral meningocele syndrome
ORPHA:2789Legius syndrome
ORPHA:137605Leigh syndrome
ORPHA:506Lelis syndrome
ORPHA:140936Leukoencephalopathy with calcifications and cysts
ORPHA:542310Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816Liddle syndrome
ORPHA:526LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369Locked-in syndrome
ORPHA:2406Lowry-Wood syndrome
ORPHA:1824LUMBAR syndrome
ORPHA:83628Lynch syndrome
ORPHA:144Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Matthew-Wood syndrome
ORPHA:2470Maxillonasal dysplasia
ORPHA:1248Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Metaphyseal acroscyphodysplasia
ORPHA:1240Microphthalmia with linear skin defects syndrome
ORPHA:2556Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112