Distal 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-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
ORPHA:314555FATCO syndrome
ORPHA:2492Female restricted epilepsy with intellectual disability
ORPHA:101039Focal facial dermal dysplasia type I
ORPHA:79133Fowler urethral sphincter dysfunction syndrome
ORPHA:2795Frank-Ter Haar syndrome
ORPHA:137834Fraser syndrome
ORPHA:2052Frasier syndrome
ORPHA:347Gardner syndrome
ORPHA:79665GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569Haddad syndrome
ORPHA:99803HANAC syndrome
ORPHA:73229HARP syndrome
ORPHA:157855Harrod syndrome
ORPHA:2115Heart-hand syndrome
ORPHA:228184HEC syndrome
ORPHA:2119Heiner syndrome
ORPHA:99932HELLP syndrome
ORPHA:244242Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hemiparkinsonism-hemiatrophy syndrome
ORPHA:306669Hennekam syndrome
ORPHA:2136HERNS syndrome
ORPHA:63261HIDEA syndrome
ORPHA:436141Hinman syndrome
ORPHA:84085Holmes-Adie syndrome
ORPHA:454718Huriez syndrome
ORPHA:384Hurler syndrome
ORPHA:93473Hurler-Scheie syndrome
ORPHA:93476Hyper-IgE syndrome
ORPHA:331223Hyperimmunoglobulinemia D with periodic fever
ORPHA:343Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
ORPHA:363694Hypoglossia-hypodactyly syndrome
ORPHA:989Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome
ORPHA:528105Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637