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Tyrosinemia, Type II |
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richner-hanhart syndrom oculocutan type tyrosinosi oculocutaneous type tyrosinosi oculocutaneous type tyrosinosis deficiency, 4-hydroxyphenylpyruvate dioxygenas deficiency, 4-hydroxyphenylpyruvate dioxygenase hepatorenal tyrosinemias 2 tyrosinemias, typ deficiency disease, fumarylacetoacetas deficiency disease, fumarylacetoacetase deficiencies, tat type ii tyrosinemia deficiency, tat dioxygenase deficiencies, 4-hydroxyphenylpyruvate tyrosinemia, type 2 tyrosinemia, type i 4 hydroxyphenol pyruv acid oxidas defici disea 4 hydroxyphenol pyruv acid oxidas defici diseas tyrosinemias fumarylacetoacetase deficiency oculocutan type tyrosino oculocutan type tyrosinos tyrosinemia, type i i tyrosinosis, oculocutaneous typ hepatoren tyrosinemia dioxygenas deficiencies, 4-hydroxyphenylpyruv hereditary tyrosinemia, type i hereditary tyrosinemia, type ii tat deficiency disease, fumarylacetoacetase defici deficiency disease, tyrosine transaminas deficiency disease, tyrosine transaminase tyrosinoses, oculocutan typ tyrosinemias, hepatorenal tyrosinemia type 1 tyrosinemia type 1s 4-hydroxyphenylpyruv acid oxidas defici fumarylacetoacetase deficiencies deficiency, fumarylacetoacetas deficiency, fumarylacetoacetase keratosis palmoplantaris with corneal dystrophi keratosis palmoplantaris with corneal dystrophy tyrosine transaminase defici deficiencies, fumarylacetoaceta tyrosinemia fumarylacetoacetase deficiency diseas deficiency disease, 4 hydroxyphenol pyruvic acid oxidase diseases, fumarylacetoacetas defici deficiencies, 4-hydroxyphenylpyruv dioxygena deficiencies, 4-hydroxyphenylpyruv dioxygenas richner hanhart syndrom type ii tyrosinemias richner-hanhart syndrome, tyrosinosis, oculocutan typ richner-hanhart syndrome, tyrosinosis, oculocutan type tyrosine aminotransferase deficiency fumarylacetoacetas defici disea deficiencies, 4-hydroxyphenylpyruvate dioxygenas deficiencies, 4-hydroxyphenylpyruvate dioxygenase type tyrosinoses, oculocutaneous diseases, fumarylacetoacetase defici richner-hanhart syndrome, tyrosinosis, oculocutaneous type tyrosinemia, hepatoren tyrosinoses, oculocutaneous typ tyrosinoses, oculocutaneous type tyrosine transaminase deficiency diseas type i hypertyrosinemias type i tyrosinemia type i tyrosinemias dioxygenase deficiencies, 4-hydroxyphenylpyruv 4-hydroxyphenylpyruvic acid oxidase defici deficiency disease, 4-hydroxyphenol pyruvic acid oxidas fumarylacetoacetase defici tyrosine aminotransferase defici diseases, fumarylacetoacetase deficiency tyrosinemia, type ii tyrosinemia, type iii type tyrosinosis, oculocutan 4 hydroxyphenylpyruv dioxygenas defici disea 4 hydroxyphenylpyruv dioxygenas defici diseas hepatorenal tyrosinemia dioxygenase deficiency, 4-hydroxyphenylpyruvate deficiencies, fumarylacetoacetase deficiencies, fumarylacetoacetas tyrosinemias, type iii hereditari tyrosinemia, type iii tyrosin transaminas defici disea tyrosin transaminas defici diseas type tyrosinosis, oculocutaneous fumarylacetoacetas defici diseas dioxygenase deficiency, 4-hydroxyphenylpyruv deficiency diseases, fumarylacetoacetas tyrosin transaminas defici 4-hydroxyphenol pyruvic acid oxidase deficiency diseas 4-hydroxyphenol pyruvic acid oxidase deficiency disease richner hanhart syndrome deficiency, fumarylacetoaceta syndrome, richner-hanhart tyrosinemia, hereditari tyrosinemia, hereditary type i hypertyrosinemia hereditari tyrosinemia tyrosinemias, hereditari oculocutaneous type tyrosinos 4-hydroxyphenol pyruv acid oxidas defici disea 4-hydroxyphenol pyruv acid oxidas defici diseas tyrosinemias, hepatoren tyrosinemias, type 2 4 hydroxyphenylpyruvate dioxygenase deficiency disease defici disease, fumarylacetoaceta tyrosinemia, hepatorenal disease, fumarylacetoacetase deficiency defici disease, tyrosin transamina defici disease, tyrosin transaminas tyrosinemias, type i tyrosinemias, type ii richner-hanhart syndromes richner-hanhart syndrome 2 tyrosinemias, type tyrosine transaminase deficiency disease tyrosinosis, oculocutaneous type hypertyrosinemia, type i fumarylacetoacetase deficiency disease fumarylacetoacetase deficiency diseases oculocutaneous type tyrosinoses defici disease, fumarylacetoacetas type tyrosinoses, oculocutan tyrosine transaminase deficiency defici diseases, fumarylacetoaceta defici diseases, fumarylacetoacetas hypertyrosinemias, type i 4-hydroxyphenylpyruvate dioxygenase deficiency hypertyrosinemia type iii tyrosinemia type iii tyrosinemias tyrosinosis, oculocutan type tyrosinoses, oculocutan type type 2 tyrosinemia type 2 tyrosinemias richner-hanhart syndrome, tyrosinosis, oculocutaneous typ 4-hydroxyphenylpyruv dioxygenas defici deficiency disease, 4 hydroxyphenol pyruvic acid oxidas 4 hydroxyphenol pyruvic acid oxidase deficiency diseas 4 hydroxyphenol pyruvic acid oxidase deficiency disease defici disease, 4 hydroxyphenol pyruv acid oxida defici disease, 4 hydroxyphenol pyruv acid oxidas 4-hydroxyphenylpyruvic acid oxidase deficiency deficiency disease, 4-hydroxyphenol pyruvic acid oxidase dioxygenas deficiency, 4-hydroxyphenylpyruv hereditari tyrosinemia, type i hereditari tyrosinemia, type ii tat deficiencies deficiency, 4-hydroxyphenylpyruv dioxygena deficiency, 4-hydroxyphenylpyruv dioxygenas defici disease, 4-hydroxyphenol pyruv acid oxida defici disease, 4-hydroxyphenol pyruv acid oxidas hereditary tyrosinemia, type iii 4-hydroxyphenylpyruvate dioxygenase defici disease, fumarylacetoacetas defici hereditary tyrosinemia hereditary tyrosinemias deficiency diseases, fumarylacetoacetase tyrosinosis, oculocutan typ oregon type tyrosinemia tyrosinemias, hereditary fumarylacetoacetas defici syndromes, richner-hanhart keratosi palmoplantari with corneal dystrophi tyrosin aminotransferas defici 4 hydroxyphenylpyruvate dioxygenase deficiency diseas tat defici |
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http://id.nlm.nih.gov/mesh/D020176 |
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richner-hanhart syndrom oculocutan type tyrosinosi oculocutaneous type tyrosinosi oculocutaneous type tyrosinosis deficiency, 4-hydroxyphenylpyruvate dioxygenas deficiency, 4-hydroxyphenylpyruvate dioxygenase hepatorenal tyrosinemias 2 tyrosinemias, typ deficiency disease, fumarylacetoacetas deficiency disease, fumarylacetoacetase deficiencies, tat type ii tyrosinemia deficiency, tat dioxygenase deficiencies, 4-hydroxyphenylpyruvate tyrosinemia, type 2 tyrosinemia, type i 4 hydroxyphenol pyruv acid oxidas defici disea 4 hydroxyphenol pyruv acid oxidas defici diseas tyrosinemias fumarylacetoacetase deficiency oculocutan type tyrosino oculocutan type tyrosinos tyrosinemia, type i i tyrosinosis, oculocutaneous typ hepatoren tyrosinemia dioxygenas deficiencies, 4-hydroxyphenylpyruv hereditary tyrosinemia, type i hereditary tyrosinemia, type ii tat deficiency disease, fumarylacetoacetase defici deficiency disease, tyrosine transaminas deficiency disease, tyrosine transaminase tyrosinoses, oculocutan typ tyrosinemias, hepatorenal tyrosinemia type 1 tyrosinemia type 1s 4-hydroxyphenylpyruv acid oxidas defici fumarylacetoacetase deficiencies deficiency, fumarylacetoacetas deficiency, fumarylacetoacetase keratosis palmoplantaris with corneal dystrophi keratosis palmoplantaris with corneal dystrophy tyrosine transaminase defici deficiencies, fumarylacetoaceta tyrosinemia fumarylacetoacetase deficiency diseas deficiency disease, 4 hydroxyphenol pyruvic acid oxidase diseases, fumarylacetoacetas defici deficiencies, 4-hydroxyphenylpyruv dioxygena deficiencies, 4-hydroxyphenylpyruv dioxygenas richner hanhart syndrom type ii tyrosinemias richner-hanhart syndrome, tyrosinosis, oculocutan typ richner-hanhart syndrome, tyrosinosis, oculocutan type tyrosine aminotransferase deficiency fumarylacetoacetas defici disea deficiencies, 4-hydroxyphenylpyruvate dioxygenas deficiencies, 4-hydroxyphenylpyruvate dioxygenase type tyrosinoses, oculocutaneous diseases, fumarylacetoacetase defici richner-hanhart syndrome, tyrosinosis, oculocutaneous type tyrosinemia, hepatoren tyrosinoses, oculocutaneous typ tyrosinoses, oculocutaneous type tyrosine transaminase deficiency diseas type i hypertyrosinemias type i tyrosinemia type i tyrosinemias dioxygenase deficiencies, 4-hydroxyphenylpyruv 4-hydroxyphenylpyruvic acid oxidase defici deficiency disease, 4-hydroxyphenol pyruvic acid oxidas fumarylacetoacetase defici tyrosine aminotransferase defici diseases, fumarylacetoacetase deficiency tyrosinemia, type ii tyrosinemia, type iii type tyrosinosis, oculocutan 4 hydroxyphenylpyruv dioxygenas defici disea 4 hydroxyphenylpyruv dioxygenas defici diseas hepatorenal tyrosinemia dioxygenase deficiency, 4-hydroxyphenylpyruvate deficiencies, fumarylacetoacetase deficiencies, fumarylacetoacetas tyrosinemias, type iii hereditari tyrosinemia, type iii tyrosin transaminas defici disea tyrosin transaminas defici diseas type tyrosinosis, oculocutaneous fumarylacetoacetas defici diseas dioxygenase deficiency, 4-hydroxyphenylpyruv deficiency diseases, fumarylacetoacetas tyrosin transaminas defici 4-hydroxyphenol pyruvic acid oxidase deficiency diseas 4-hydroxyphenol pyruvic acid oxidase deficiency disease richner hanhart syndrome deficiency, fumarylacetoaceta syndrome, richner-hanhart tyrosinemia, hereditari tyrosinemia, hereditary type i hypertyrosinemia hereditari tyrosinemia tyrosinemias, hereditari oculocutaneous type tyrosinos 4-hydroxyphenol pyruv acid oxidas defici disea 4-hydroxyphenol pyruv acid oxidas defici diseas tyrosinemias, hepatoren tyrosinemias, type 2 4 hydroxyphenylpyruvate dioxygenase deficiency disease defici disease, fumarylacetoaceta tyrosinemia, hepatorenal disease, fumarylacetoacetase deficiency defici disease, tyrosin transamina defici disease, tyrosin transaminas tyrosinemias, type i tyrosinemias, type ii richner-hanhart syndromes richner-hanhart syndrome 2 tyrosinemias, type tyrosine transaminase deficiency disease tyrosinosis, oculocutaneous type hypertyrosinemia, type i fumarylacetoacetase deficiency disease fumarylacetoacetase deficiency diseases oculocutaneous type tyrosinoses defici disease, fumarylacetoacetas type tyrosinoses, oculocutan tyrosine transaminase deficiency defici diseases, fumarylacetoaceta defici diseases, fumarylacetoacetas hypertyrosinemias, type i 4-hydroxyphenylpyruvate dioxygenase deficiency hypertyrosinemia type iii tyrosinemia type iii tyrosinemias tyrosinosis, oculocutan type tyrosinoses, oculocutan type type 2 tyrosinemia type 2 tyrosinemias richner-hanhart syndrome, tyrosinosis, oculocutaneous typ 4-hydroxyphenylpyruv dioxygenas defici deficiency disease, 4 hydroxyphenol pyruvic acid oxidas 4 hydroxyphenol pyruvic acid oxidase deficiency diseas 4 hydroxyphenol pyruvic acid oxidase deficiency disease defici disease, 4 hydroxyphenol pyruv acid oxida defici disease, 4 hydroxyphenol pyruv acid oxidas 4-hydroxyphenylpyruvic acid oxidase deficiency deficiency disease, 4-hydroxyphenol pyruvic acid oxidase dioxygenas deficiency, 4-hydroxyphenylpyruv hereditari tyrosinemia, type i hereditari tyrosinemia, type ii tat deficiencies deficiency, 4-hydroxyphenylpyruv dioxygena deficiency, 4-hydroxyphenylpyruv dioxygenas defici disease, 4-hydroxyphenol pyruv acid oxida defici disease, 4-hydroxyphenol pyruv acid oxidas hereditary tyrosinemia, type iii 4-hydroxyphenylpyruvate dioxygenase defici disease, fumarylacetoacetas defici hereditary tyrosinemia hereditary tyrosinemias deficiency diseases, fumarylacetoacetase tyrosinosis, oculocutan typ oregon type tyrosinemia tyrosinemias, hereditary fumarylacetoacetas defici syndromes, richner-hanhart keratosi palmoplantari with corneal dystrophi tyrosin aminotransferas defici 4 hydroxyphenylpyruvate dioxygenase deficiency diseas tat defici |
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Tyrosinemia, Type II |
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MeSH:D020176 |
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Tyrosinemia, Type II |
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