HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Holmes-Adie syndrome
ORPHA:454718Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypocomplementemic urticarial vasculitis
ORPHA:36412Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237Hypotonia-speech impairment-severe cognitive delay syndrome
ORPHA:371364IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268ICHAD syndrome
ORPHA:699599Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Ichthyosis-hypotrichosis syndrome
ORPHA:91132IMAGe syndrome
ORPHA:85173Infantile convulsions and choreoathetosis
ORPHA:31709Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome
ORPHA:1495Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
ORPHA:306504IRIDA syndrome
ORPHA:209981Iridocorneal endothelial syndrome
ORPHA:64734IRVAN syndrome
ORPHA:209943Isaacs syndrome
ORPHA:84142IVIC syndrome
ORPHA:2307JMP syndrome
ORPHA:324999KBG 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:1187Locked-in syndrome
ORPHA:2406Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 5p syndrome
ORPHA:281Monosomy 9p syndrome
ORPHA:261112Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Musculocontractural Ehlers-Danlos syndrome
ORPHA:2953