| Ungerska | Svenska medicinsk |
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| Ellis-van Creveld-szindróma [f.r.] [chondroectodermalis dysplasia] infoEllis-van Creveld syndrome, chondroectodermal dysplasia, a genetic, autosomal recessive condition, the cartilage converts to bone while growing, dwarfism | Ellis-van Creveld-syndrom -et - |
| chondroectodermalis dysplasia [chondroectodermal dysplasia] infochondroectodermal dysplasia, Ellis-Van Creveld syndrome, a rare autosomal recessive congenital abnormality | kondroektodermal dysplasi |
| chondroectodermalis dysplasia [dysplasia chondroectodermalis] infochondroectodermal dysplasia, the cartilage converts to bone while growing | chondroectodermal dysplasi |
| ranchiootorenal dysplasia · branchio-otorenális-szindróma [syndroma branchiootorenalis] infobranchiootorenal [BOR] syndrome, Melnick-Fraser syndrome, a condition that disrupts the development of tissues in the neck and causes malformations of the ears and kidneys | brankiootorenalt syndrom [BOR]infobrankiootorenal dysplasi, Melnick-Frasers syndrom |
| Christ-Siemens-Touraine-szindróma · ectodermalis dysplasia · külső csíralemez hibás fejlődése [dysplasia ectodermalis] infoChrist-Siemens-Touraine syndrome, ectodermal dysplasia, ED, defective development of the outer germinal plate | ektodermal dysplasi |
| Marshall-szindróma infoPFAPA, periodic fever, aphthous stomatitis, pharyngitis, adenitis, a childhood syndrome | PFAPA |
| Andogsky szindróma [cataracta dermatogenes, cataracta syndermatotica] infodevelopment of total soft cataracts in adults who have a history of chronic dermatologic eczema, dermatogenic cataract | Andogsky syndrominfoatopisk dermatit o. grå starr |
| Broadbent-szindróma [R] infoBroadbent syndrome, massive subarachnoid haemorrhage which ruptures into the ventricular system | Broadbent syndrom |
| paraneoplasztikus-szindróma [syndroma paraneoplastica] infoparaneoplastic-syndrome, a syndrome that is the consequence of a tumor in the body [usually a cancerous one] | paraneoplastiskt syndrom |
| Morris-szindróma [férfi álhermafroditizmus] [feminisatio testicularis, endohermaphroditismus] infoMorris syndrome, X-linked recessive condition due to a complete or partial insensitivity to androgens, individuals with testes but of female phenotype | testikulär feminiseringinfoindivider med testiklar men av kvinnlig fenotyp |
| triád-szindróma [gyomorizomzat részleges v. teljes hiánya, kétoldali kriptorchidizmus, húgyúti rendellenességek] infoPrune Belly syndrome, Eagle-Barrett syndrome, triad syndrome, a rare congenital disorder, the triad of deficient abdominal musculature, cryptorchidism, and urinary tract abnormalities | triad syndrom |
| Zieve-szindróma infoZieve's syndrome [ZS] is a triad of jaundice, hemolytic anemia, and hyperlipidemia | Zieve-syndrom -et - |
| Leschke-szindróma infoLeschke syndrome, growth retardation, intellectual disability, diabetes mellitus, genital hypoplasia, hyperthyroidism | Leschke syndrominfooförklarad ärftlig pigment dystrofi |
| Bartter-szindróma [hyperaldosteronismus] infoBartter syndrome [BS], renal tubular salt-wasting disorders in which the kidneys cannot reabsorb chloride in the loop of Henle [TALH] | Bartters syndrom |
| lipodystrophia-szindróma [lipodystrophia intestinalis] infolipodystrophy syndrome, group of disorders characterized by either generalized or partial lack of adipose tissue | lipodystrofisyndrom -et - |
| Calvé-szindróma [syndroma Calvei] infoCalvé syndrome | Calvé syndrominfoaseptisk epiphysealnekros i kotkroppen |
| Cushing-szindróma [syndroma Cushingi] infoCushing syndrome [buffalo hump, striae] | Cushings syndrom |
| Determann-szindróma [izomműködési zavar érelmeszesedésben] [syndroma Determanni] infoDetermann syndrome, intermittent muscle myasthenia caused by arteriosclerosis | Determann-syndrom -et - |
| Riehl-szindróma [melanodermitis toxica, poikiloderma reticularis pigmentosa] infoRiehl syndrome, Riehl melanosis, a brown pigmentary condition of the exposed portions of the skin of the neck and face | Riehls melanos |
| Haven-szindróma infoHaven's syndrome, characterised by pain in the wrist which progresses to the shoulder, a pallor of the hand and wrist, and loss of radial pulsation. Haven attributed the condition to compression of the subclavian artery by the scalenus muscle | Haven-syndrom -et - |
| Moore-szindróma infoMoore Federman syndrome, MFS, short stature, stiffness of the joints, characteristic facies and ocular abnormalities | Moore-syndrom -et - |
| Ivemark-szindróma [f.r.] infoIvemark syndrome, a rare disorder that affects multiple organ systems of the body, asplenia, hypoplasia] of the spleen, malformations of the heart and the abnormal arrangement of the internal organs of the chest and abdomen | Ivemark syndrom |
| Scheie-szindróma infoScheie syndrome, a rare genetic lysosomal storage problem with an increased prevalence of carpal tunnel syndrome, CTS, in adolescence | Scheies syndrom |
| Wright-szindróma infoWright syndrome, circulatory disorder occurring in the limb in hyper-abduction of the arm | Wright-syndrom -et - |
| Dupuytren-szindróma [fibromatosis palmaris] infopalmar fibromatosis, Dupuytren's contracture, viking disease, hereditary condition, shortening, thickening, and fibrosis of the palmar fascia producing a flexion deformity of a finger | vikingasjukan |
| Asperger-szindróma infoAsperger's syndrome, Asperger's, [AS], autism spectrum disorder [ASD] | Asperger syndrom [ASD] |
| Parhon-szindróma infoParhon syndrome,syndrome of inappropriate antidiuretic hormone secretion, SIADH | Parhon-syndrom -et - |
| Brandt-szindróma [f.r.] [acrodermatitis enteropathica] infoBrandt syndrome, congenital zinc deficiency | Brandt syndrominfoen typ av acrodermatitis inträffar i barndomen |
| Bernuth-szindróma [syndroma Bernuthi] infoBernuth syndrome, sporadic hemophilia | Bernuth syndrom |
| Moebius-szindróma [f.r.] [congenitalis facialis diplegia] infoMoebius syndrome, congenital facial diplegia, associated with bilateral abducens nerve palsy | Möbius sekvensinfoavvikelser som har uppstatt till följd av en yttre orsak |
| Hageman-szindróma infofactor XII Deficiency, a deficiency of the factor XII [Hageman factor] | Hagemanfaktorbrist -en -erinfoF12-brist, faktor XII-brist, HAF-brist, Hageman-drag |
| Poland-szindróma [f.r.] [Poland syndroma, agenesia musculus pectoralis maior, pectoral dysplasia-dysdactyly] infoPoland syndrome, a child is born with missing or underdeveloped chest muscles | Poland-syndrom -et - |
| Takahara-szindróma [f.r.] [acatalasaemia] infoTakahara's, disease, congenital absence of catalase enzuyme | Takahara-syndrom -et - |
| Behr-szindróma [syndroma Behri] infoBehr syndrome, early-onset optic atrophy along with neurological features [ataxia, spasticity, intellectual disability] | Behr syndrom |
| Dzierzynsky-szindróma [dystrophia periostalis hyperplastica familiaris] infoDzierzynsky syndrome, familial hyperplastic periosteal dystrophy | Dzierzynsky syndrom |
| Roemheld-szindróma infoRoemheld syndrome, abdominal maladies triggering reflexes in the heart, triggered by excessive gas accumulation in the gastrointestinal tract | Roemheld syndrominfogastrokardialt symtomkomplex, gastrointestinala störningar som orsakas av hjärtproblem |
| Launois-szindróma infoLaunois-Bensaude syndrome, disorder by painless symmetrical diffuse deposits of fat beneath the skin of the neck, upper trunk, arms and legs | Launois-syndrom -et - |
| Eisenmenger-szindróma [f.r.] [Eisenmenger syndroma] infoEisenmenger syndrome, a long-term complication of an unrepaired heart problem present at birth | Eisenmengers syndrom |
| Paxton-szindróma [P: Corynebacterium tenuis, C. propinguum, C flavescens, Serratia marcescens] infoPaxton disease, trichomycosis, bacterial infection that affects your skin and hair in the armpit | trichomycosis -infotrichobacteriosis |
| orofaciodigitalis-szindróma infooral-facial-digital syndrome, OFDS, Mohr syndrome, Papillon-Léage-Psaume Syndrome, a group of conditions that affect the development of their oral cavity [mouth, tongue, teeth, and jaw], face [head, eyes and nose] and finger and toes [digits] | orofaciodigitalt syndrom [OFD]infoPapillon Léage-Psaumes syndrom [OFD I], Mohrs syndrom [OFD II] |
