Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Familial isolated café-au-lait macules
ORPHA:2678GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypomyelination-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:31709Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
ORPHA:306504Inverted duplicated chromosome 15 syndrome
ORPHA:3306IRIDA syndrome
ORPHA:209981Iridocorneal endothelial syndrome
ORPHA:64734IRVAN syndrome
ORPHA:209943Isaacs syndrome
ORPHA:84142Isochromosome Y syndrome
ORPHA:96325Isochromosomy Yp syndrome
ORPHA:98797Isochromosomy Yq syndrome
ORPHA:98798Isotretinoin syndrome
ORPHA:2305IVIC syndrome
ORPHA:2307JMP syndrome
ORPHA:324999Kabuki syndrome
ORPHA:2322Kahrizi syndrome
ORPHA:168972KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome
ORPHA:457193KBG syndrome
ORPHA:2332Keipert syndrome
ORPHA:2662Kenny-Caffey syndrome
ORPHA:2333Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
ORPHA:281201Keutel syndrome
ORPHA:85202KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908Kjellin syndrome
ORPHA:100996L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lymphedema-atrial septal defects-facial changes syndrome
ORPHA:86915Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649