hereditary
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hereditary- hereditary ferritinopathy
- hereditary thrombophilia
- hereditary aceruloplasminemia
- stomatocytosis, hereditary
- hereditary xerocytosis
- hereditary arthro-ophthalmopathy, hereditary progressive arthro-ophthalmopathy
- coproporphyria, hereditary coproporphyria
- hereditary alpha-tryptasemia
- disease
- chorea
- nephritis
- deafness
- elliptocytosis
- cardiomyopathy
- hereditary breast and ovarian cancer syndrome
- angioedema
- cancer
- paraplegia
- impairment
- dystrophy
- telangiectasia, telangiectasis
- dysplasia
- spherocytosis
- genodermatosis
- heritable
- neuropathy
- Leber, Theodor
- plasmagene
- xerocyte
- acquired
- Upshaw-Schulman Syndrome
- multiallelic
- Troyer syndrome
- germline genetic testing
- Marie, Pierre
- Rendu-Osler-Weber syndrome
- dessicocytosis
- myopathy
- Milroy disease
- index case
- arthrodysplasia
- oligodontia
- transgenic
- dentinogenesis
- dysostosis
- pharmacogenetics
- stomatocyte
- histidinemia
- eosin-5-maleimide test
- osteopoikilosis
- poliosis
- methemoglobinemia
- cystathioninuria
- anemia
- oculocerebrorenal syndrome
- Leri pleonosteosis
- 1strain
- Kartagener syndrome
- exostosis
- salpingo-oophorectomy
- deficiency
- genotype
- chondrodysplasia
- Brugada syndrome
- oxalosis
- acrokeratosis verruciformis
- autohemolysis test
- cystinuria
- mastectomy
- choroideremia
- pseudohypoparathyroidism
- neuroferritinopathy
- argininosuccinicaciduria
- elliptocyte
- pachydermoperiostosis
- handedness
- penetrance
- bank
- alopecia
- dwarfism
- Amsterdam criteria
- Stickler syndrome
- Alport syndrome
- mapping
- retinitis
- favism
- thalassemia
- methemoglobin
- leukodystrophy
- keratoconus
- amelogenesis
- transient hypoglobulinemia
- retinoblastoma
- fructose intolerance