Hypotonia-speech impairment-severe cognitive delay syndrome
ORPHA:371364Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936IBIDS 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:306504IRIDA syndrome
ORPHA:209981Iridocorneal endothelial syndrome
ORPHA:64734IRVAN syndrome
ORPHA:209943Isaacs syndrome
ORPHA:84142Isolated hemihyperplasia
ORPHA:2128IVIC syndrome
ORPHA:2307JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332Keipert syndrome
ORPHA:2662KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Maxillonasal dysplasia
ORPHA:1248Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Miller Fisher syndrome
ORPHA:98919Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mucopolysaccharidosis type 2
ORPHA:580Mucopolysaccharidosis type 2, attenuated form
ORPHA:217093Mucopolysaccharidosis type 2, severe form
ORPHA:217085Multiple endocrine neoplasia type 1
ORPHA:652Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087Nager syndrome
ORPHA:245NAME syndrome
ORPHA:623Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Non-24-hour sleep-wake syndrome
ORPHA:73267