Hypomyelination-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:84142IVIC syndrome
ORPHA:2307JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laron syndrome
ORPHA:633Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lateral meningocele syndrome
ORPHA:2789Lesch-Nyhan syndrome
ORPHA:510Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816LIG4 syndrome
ORPHA:99812Lujan-Fryns syndrome
ORPHA:776Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Marfan syndrome
ORPHA:558Maxillonasal dysplasia
ORPHA:1248Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479MEPAN syndrome
ORPHA:508093Metaphyseal acroscyphodysplasia
ORPHA:1240Microphthalmia with linear skin defects syndrome
ORPHA:2556Mietens syndrome
ORPHA:2557Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Morvan syndrome
ORPHA:83467Moynahan syndrome
ORPHA:2574Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841