Focal facial dermal dysplasia type I
ORPHA:79133Fragile X syndrome
ORPHA:908Frey syndrome
ORPHA:662240GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Guillain-Barré syndrome
ORPHA:2103H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hereditary hyperekplexia
ORPHA:3197Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Intellectual disability-early-onset cataract-microcephaly syndrome
ORPHA:633035Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome
ORPHA:457193KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
ORPHA:2698L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816LIG4 syndrome
ORPHA:99812LUMBAR syndrome
ORPHA:83628Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466Maxillonasal dysplasia
ORPHA:1248Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Metaphyseal acroscyphodysplasia
ORPHA:1240Microcornea-myopic chorioretinal atrophy-telecanthus syndrome
ORPHA:369970Microphthalmia with linear skin defects syndrome
ORPHA:2556Monoamine 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:69087