Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816LIG4 syndrome
ORPHA:99812Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715Maxillonasal dysplasia
ORPHA:1248Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Metaphyseal acroscyphodysplasia
ORPHA:1240Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Mixed connective tissue disease
ORPHA:809MOMO syndrome
ORPHA:2563Monoamine oxidase A deficiency
ORPHA:3057Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Multiple 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:69087NAME syndrome
ORPHA:623NARP syndrome
ORPHA:644Nicolau syndrome
ORPHA:664787Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculocerebrorenal syndrome of Lowe
ORPHA:534Oculodentodigital dysplasia
ORPHA:2710Oculotrichoanal syndrome
ORPHA:2717Odontomatosis-aortae esophagus stenosis syndrome
ORPHA:2724Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183