Traduction de «disease methaemoglobinaemia hereditary » (Anglais → Néerlandais) :

Congenital NADH-methaemoglobin reductase deficiency Haemoglobin-M [Hb-M] disease Methaemoglobinaemia, hereditary
congenitale deficiëntie van NADH-methemoglobinereductase | hemoglobine M-ziekte [Hb M-ziekte] | methemoglobinemie, hereditair

Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas
heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]

chronic progressive hereditary chorea | Huntington chorea | Huntington disease | Huntington's chorea | Huntington's disease | HD [Abbr.]
chorea van Huntington | ziekte van Huntington

hereditary disease linked with the sex
geslachtsgebonden erfelijke ziekte

Hereditary mixed polyposis syndrome (HMPS) describes an autosomal dominantly inherited large-bowel disease with characteristics of the presence of a mixture of hyperplastic, atypical juvenile and adenomatous polyps that are associated with an increas
hereditary mixed polyposis syndrome

A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST), pulmonary chondromas and extraadrenal paragangliomas. Less than 100 cases have been reported worldwide. The disease primarily affects young women (mean age of o
Carney-triade

Bernard-Soulier [giant platelet] syndrome Glanzmann's disease Grey platelet syndrome Thromboasthenia (haemorrhagic)(hereditary) Thrombocytopathy
grey platelet syndrome | syndroom van Bernard-Soulier [giant platelet syndrome] | trombasthenie (hemorragisch)(hereditair) | trombocytopathie | ziekte van Glanzmann

Hereditary cerebellar:ataxia NOS | degeneration | disease | syndrome
hereditair(e) cerebellair(e) | ataxie NNO | hereditair(e) cerebellair(e) | degeneratie | hereditair(e) cerebellair(e) | syndroom | hereditair(e) cerebellair(e) | ziekte

A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese
syndroom van Buschke-Fischer-Brauer