Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Heiner syndrome
ORPHA:99932Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hurler syndrome
ORPHA:93473Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome
ORPHA:684216Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Leukoencephalopathy with calcifications and cysts
ORPHA:542310Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Maxillonasal dysplasia
ORPHA:1248Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Metaphyseal acroscyphodysplasia
ORPHA:1240Microphthalmia with linear skin defects syndrome
ORPHA:2556Miller Fisher syndrome
ORPHA:98919Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mucopolysaccharidosis 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:623Nephrosis-deafness-urinary tract-digital malformations syndrome
ORPHA:2669Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972