Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Hereditary vitamin B12 deficiency anaemia (Q39488) (← links)
- Megaloblastic anaemia due to vitamin B12 deficiency (Q39489) (← links)
- Folate deficiency anaemia due to decreased intestinal absorption (Q39490) (← links)
- Folate deficiency anaemia due to low intake (Q39491) (← links)
- Drug-induced folate deficiency anaemia (Q39492) (← links)
- Folate deficiency anaemia due to increased requirements (Q39493) (← links)
- Hereditary folate deficiency anaemia (Q39494) (← links)
- Folate deficiency anaemia (Q39495) (← links)
- Hereditary orotic aciduria (Q39496) (← links)
- Protein deficiency anaemia (Q39497) (← links)
- Scorbutic anaemia (Q39498) (← links)
- Acquired pyridoxine deficiency anaemia (Q39499) (← links)
- Acquired vitamin A deficiency anaemia (Q39500) (← links)
- Acquired thiamine deficiency anaemia (Q39501) (← links)
- Copper deficiency anaemia (Q39502) (← links)
- Acquired riboflavin deficiency anaemia (Q39503) (← links)
- Acquired vitamin E deficiency anaemia (Q39504) (← links)
- Acquired other vitamin B deficiency anaemia (Q39505) (← links)
- Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency (Q39506) (← links)
- Haemolytic anaemias due to hexose monophosphate shunt or glutathione metabolism anomalies (Q39507) (← links)
- Haemolytic anaemia due to adenosine deaminase excess (Q39508) (← links)
- Hereditary haemolytic anaemia (Q39510) (← links)
- Alpha thalassaemia related syndromes (Q39511) (← links)
- Thalassaemias (Q39512) (← links)
- Thalassaemic alpha-chain variants (Q39513) (← links)
- Haemoglobin H disease (– α/– – included) (Q39514) (← links)
- Alpha thalassaemia (Q39515) (← links)
- Hemoglobin Bart's fetalis syndrome (Q39516) (← links)
- Beta thalassaemia (Q39517) (← links)
- Delta, delta-beta or gamma-delta-beta thalassaemia (Q39518) (← links)
- Mild alpha thalassaemia diseases (Q39519) (← links)
- Hereditary persistence of fetal haemoglobin (Q39520) (← links)
- Haemoglobin C/beta thalassaemia compound heterozygosity (Q39521) (← links)
- Haemoglobin E disease (Q39522) (← links)
- Sickle cell disorders or other haemoglobinopathies (Q39523) (← links)
- Compound heterozygous sickling disorders with crisis (Q39524) (← links)
- Low affinity haemoglobin (Q39525) (← links)
- Haemoglobin D disease (Q39526) (← links)
- Haemoglobin C disease (Q39527) (← links)
- Haemoglobin O disease (Q39528) (← links)
- High affinity haemoglobin (Q39529) (← links)
- Sickle cell disease with crisis (Q39530) (← links)
- Sickle cell disease without crisis (Q39531) (← links)
- Compound heterozygous sickling disorders without crisis (Q39532) (← links)
- Sickle cell trait (Q39533) (← links)
- Hereditary elliptocytosis (Q39534) (← links)
- Familial pseudohyperkalaemia (Q39535) (← links)
- Autoimmune haemolytic anaemia, mixed type, cold and warm (Q39536) (← links)
- Alloimmune haemolytic anaemia (Q39537) (← links)
- Acquired haemolytic anaemia, non-immune (Q39538) (← links)
