familial pyridoxine-responsive anemia
fa·mil·i·al pyr·i·dox·ine-re·spon·sive a·ne·mi·a
[MIM*206000]a rare autosomal recessive hereditary hypochromic anemia; responsive to pyridoxine.
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- familial juvenile nephrophthisis
- familial lipoprotein lipase deficiency
- familial lipoprotein lipase inhibitor
- familial malignancy
- familial Mediterranean fever
- familial Mediterranean fever, autosomal dominant
- familial medullary thyroid cancer
- familial metaphyseal dysostosis
- familial microcytic anemia
- familial multiple endocrine
- familial nephrosis
- familial nonhemolytic jaundice
- familial osteochondrodystrophy
- familial paroxysmal polyserositis
- familial paroxysmal rhabdomyolysis
- familial partial lipodystrophy
- familial partial lipodystrophy type 3
- familial periodic fever
- familial periodic paralysis
- familial polyendocrine adenomatosis
- familial polyposis
- familial porphyria cutanea tarda
- familial progressive hyperpigmentation
- familial pseudoinflammatory macular degeneration
- familial pseudoinflammatory maculopathy
- familial pyridoxine-responsive anemia
- familial recurrent polyserositis
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- familial short stature
- familial spinal muscular atrophy
- familial spinal neurofibromatosis
- familial tremor
- familial visceral amyloidosis
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- familial polycythemia
- familial polycythemia
- familial polycythemia
- familial polycythemia
- familial polyendocrine adenomatosis
- familial polyneuropathy
- familial polyneuropathy
- Familial polyposis
- Familial polyposis
- Familial polyposis
- Familial Polyposis Coli
- Familial Polyposis Coli
- Familial Polyposis Coli
- Familial Polyposis Coli/Gardner's Syndrome
- Familial Porphyria Cutanea Tarda
- Familial Porphyria Cutanea Tarda
- familial primary lymphoedema
- familial primary lymphoedema
- familial primary lymphoedema
- familial primary lymphoedema
- familial primary lymphoedema
- familial primary pulmonary hypertension
- familial progressive hyperpigmentation
- familial progressive hyperpigmentation 2
- Familial Prostate Cancer Study
- Familial Pseudohyperkalemia
- familial pseudoinflammatory macular degeneration
- familial pseudoinflammatory maculopathy
- Familial Pulmonary Arterial Hypertension
- Familial Pure Depressive Disorder
- familial pyridoxine-responsive anemia
- familial recurrent polyserositis
- familial recurring polyserositis
- familial reflex myoclonus
- familial reflex myoclonus
- familial reflex myoclonus
- Familial relationship
- Familial relationship
- Familial relationship
- familial renal amyloidosis of Shar pei dogs
- familial renal amyloidosis of Shar pei dogs
- familial renal amyloidosis of Shar pei dogs
- Familial renal disease
- Familial renal disease
- Familial renal disease
- Familial renal glycosuria
- familial screening
- familial screening
- familial screening
- familial screening
- familial selective malabsorption syndrome
- Familial Short Stature
- Familial Short Stature
- familial situs ambiguus
- Familial spastic paraparesis
- Familial Spastic Paraplegia
- familial spastic paraplegia, autosomal dominant, 2
- familial spinal muscular atrophy
- Familial Spinal Neurofibromatosis
- Familial Spinal Neurofibromatosis
- familial splenic anemia
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