IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Ichthyosis-hypotrichosis syndrome
ORPHA:91132Incontinentia pigmenti
ORPHA:464Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908L1 syndrome
ORPHA:275543Lambert syndrome
ORPHA:1296Laryngo-onycho-cutaneous syndrome
ORPHA:2407Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816Limb body wall complex
ORPHA:2369Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Maxillonasal dysplasia
ORPHA:1248Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Mesomelic dysplasia, Nievergelt type
ORPHA:2633Microphthalmia 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:261112MRCS syndrome
ORPHA:263347Mucopolysaccharidosis type 2
ORPHA:580Multiple 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:85146Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717