Cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome
ORPHA:79482Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Familial atypical multiple mole melanoma syndrome
ORPHA:404560Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Focal stiff limb syndrome
ORPHA:443804GAPO syndrome
ORPHA:2067GMS syndrome
ORPHA:2090Gordon syndrome
ORPHA:376Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
ORPHA:221043Hydrocephaly-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:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis-hypotrichosis syndrome
ORPHA:91132Imperforate oropharynx-costovertebral anomalies syndrome
ORPHA:2759Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Juvenile hyaline fibromatosis
ORPHA:2028KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laron syndrome
ORPHA:633Laryngeal abductor paralysis-intellectual disability syndrome
ORPHA:2375Laryngo-onycho-cutaneous syndrome
ORPHA:2407Linear nevus sebaceus syndrome
ORPHA:2612LUMBAR syndrome
ORPHA:83628Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Matthew-Wood syndrome
ORPHA:2470Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479