Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Foveal hypoplasia-presenile cataract syndrome
ORPHA:2253GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hepatic veno-occlusive disease-immunodeficiency syndrome
ORPHA:79124Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
ORPHA:221043Holmes-Adie syndrome
ORPHA:454718Hydrocephaly-low insertion umbilicus syndrome
ORPHA:2184Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hyperzincemia and hypercalprotectinemia
ORPHA:251523Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Juvenile hyaline fibromatosis
ORPHA:2028KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngeal abductor paralysis-intellectual disability syndrome
ORPHA:2375Laryngo-onycho-cutaneous syndrome
ORPHA:2407LUMBAR syndrome
ORPHA:83628Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Matthew-Wood syndrome
ORPHA:2470Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Monosomy 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:623Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Otofaciocervical syndrome
ORPHA:2792