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X-linked Sideroblastic Anemia
X-linked sideroblastic anemia
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Genetic disorders
(38)
Glycogen storage disease type iib
XLSA
MASA syndrome
Becker's muscular dystrophy
Lipid storage disorder
Lipid storage disorder
Pyruvate dehydrogenase deficiency
Aicardi syndrome
Simpson-Go- labi-Behmel syndrome
McLeod syndrome
ALA dehydratase deficiency
X-linked severe combined immunodeficiency
Adrenoleuk- odystrophy
Alport syndrome
Lelis syndrome
Acrocephal- opolysyndactyly
Androgen insensitivity syndrome
Very long-chain acyl coenzyme A dehydrogenase deficiency
Barth syndrome
Recessive multiple epiphyseal dysplasia
Hemophagocytic lymphohistiocytosis
Hereditary coproporphyria
47 xyy syndrome
Variegate porphyria
Nonsyndromic deafness
Erythropoietic protoporphyria
Pearson syndrome
Spinal and bulbar muscular atrophy
Congenital erythropoietic porphyria
Thalassemia
Haemophilia
22q11.2 deletion syndrome
Dyskeratosis congenita
Beta thalassemia
Adenosine deaminase deficiency
X-linked dominant
Activated protein c resistance
Porphyria cutanea tarda
Diamond Blackfan anemia
more...
Diseases and disorders
(51)
Anemia sideroblastic
Anemias
Anonychia onychodystrophy
X-linked lymphoproliferative disease
Focal dermal hypoplasia
Focal dermal hypoplasia
X-linked hypophosphatemia
Porphyrias
Ehlers-danlos syndrome dermatosparaxis type
Factor V Leiden thrombophilia
Iron deficiency anemia
X-linked ichthyosis
Acanthoche- ilonemiasis
Scleromyxedema
Polychondritis
Agenesis of corpus callosum
Anemia, hemolytic
Refractory anemia
Atelosteogenesis type 2
Centronuclear myopathy
Pernicious anemia
Aplasia cutis congenita
Hypohidrotic ectodermal dysplasia
Hematologic disease
Hemochromatosis
CHILD syndrome
Incontinentia pigmenti
Glycogen storage disease type iib
XLSA
MASA syndrome
Becker's muscular dystrophy
Lipid storage disorder
Pyruvate dehydrogenase deficiency
Alport syndrome
Acrocephal- opolysyndactyly
Androgen insensitivity syndrome
Barth syndrome
Hemophagocytic lymphohistiocytosis
Hereditary coproporphyria
47 xyy syndrome
Variegate porphyria
Pearson syndrome
Spinal and bulbar muscular atrophy
Congenital erythropoietic porphyria
Thalassemia
Haemophilia
22q11.2 deletion syndrome
Dyskeratosis congenita
Beta thalassemia
Adenosine deaminase deficiency
Activated protein c resistance
Porphyria cutanea tarda
more...
Inborn errors of metabolism
Glycogen storage disease type iib
Lipid storage disorder
Very long-chain acyl coenzyme A dehydrogenase deficiency
X-linked ichthyosis
Adenosine deaminase deficiency
Autosomal recessive disorders
(8)
Glycogen storage disease type iib
Lipid storage disorder
Very long-chain acyl coenzyme A dehydrogenase deficiency
Recessive multiple epiphyseal dysplasia
Hemophagocytic lymphohistiocytosis
Hemophagocytic lymphohistiocytosis
Congenital erythropoietic porphyria
Thalassemia
Adenosine deaminase deficiency
more...
Rare diseases
Glycogen storage disease type iib
Lipid storage disorder
Lelis syndrome
Pearson syndrome
Congenital erythropoietic porphyria
Dyskeratosis congenita
Adenosine deaminase deficiency
Porphyrias
(10)
Erythropoietic porphyrias
Hepatic porphyrias
ALA dehydratase deficiency
Acute intermittent porphyria
Erythropoietic protoporphyria
Erythropoietic protoporphyria
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Porphyria cutanea tarda
Variegate porphyria
XLSA
more...
Hematology
(14)
Red cells
Cytopenia
Microcytosis
Microcytic anemia
XLSA
XLSA
McLeod syndrome
Factor V Leiden thrombophilia
Iron deficiency anemia
Hemophagocytic lymphohistiocytosis
Anemia, hemolytic
Pernicious anemia
Hematologic disease
Hemochromatosis
Activated protein c resistance
more...
Blood disorders
(11)
Hypochromic anemia
Hematological malignancy
Macrocytic anemia
Anemias
Hemophagocytic lymphohistiocytosis
Hemophagocytic lymphohistiocytosis
Anemia, hemolytic
Refractory anemia
Thalassemia
Haemophilia
Beta thalassemia
Diamond Blackfan anemia
more...
See also
(20)
X linked
Hyper IgM Syndrome Type 1
ALAS2
PROTO oxidase
ABCB7
ABCB7
5-aminolevulinate synthase
Heme arginate
Heme
Congenital bilateral absence of vas deferens
Normoblasts
KAL1
Porphyrin
X-linked recessive
Autosomal dominant
Autosomal recessive
Letters by alphabet
Siderosis
Pyridoxine
Congenital malformations
Juvenile myelomonocytic leukemia
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