Vitamin deficiency disorder
MONDO:0024298A disorder that is caused by the deficiency of a vitamin. The deficiency may result from either suboptimal vitamin intake or conditions that prevent the vitamin's use or absorption in the body. Representative examples include beriberi caused by thiamine deficiency, scurvy caused by vitamin C deficiency, and rickets caused by vitamin D deficiency.
Also known as: avitaminosis, vitamin deficiency, vitamin deficiency disorder, Avitaminoses, deficiencies, vitamin, deficiency, vitamin, vitamin deficiencies
146 clinical trials for this condition and its sub-types, 9 tagged with Vitamin deficiency disorder itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Vitamin deficiency disorder
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Vitamin D deficiency 89 trials
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Vitamin B deficiency 0 trials · 17 incl. sub-types
3 sub-types
- Vitamin B12 deficiency 12 trials · 15 incl. sub-types Sub-types →
- Beriberi 2 trials Sub-types →
- Pyridoxine deficiency anemia 0 trials
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Scurvy 13 trials
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Vitamin A deficiency 9 trials
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Inborn vitamin metabolic disorder 0 trials · 7 incl. sub-types
5 sub-types
- Disorders of vitamin D metabolism 0 trials · 3 incl. sub-types Sub-types →
- Inborn disorder of cobalamin metabolism and transport 1 trial · 3 incl. sub-types Sub-types →
- Cerebral folate deficiency 1 trial
- Familial isolated deficiency of vitamin E 1 trial
- Neurodegenerative syndrome due to cerebral folate transport deficiency 1 trial
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Nutritional biotin deficiency 0 trials
Most studied deeper sub-types
Methylmalonic aciduria and homocystinuria type cblC
(3)
Vitamin D hydroxylation-deficient rickets, type 1B
(3)
Methylcobalamin deficiency type cblE
(2)
Methylcobalamin deficiency type cblG
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Methylmalonic aciduria, cblA type
(2)
Hereditary intrinsic factor deficiency
(1)
Methylmalonic acidemia with homocystinuria, type cblJ
(1)
Methylmalonic aciduria and homocystinuria
(1)
Methylmalonic aciduria and homocystinuria type cblF
(1)
Methylmalonic aciduria, cblB type
(1)
Transcobalamin II deficiency
(1)
Dry beriberi
(0)
Homocystinuria-megaloblastic anemia cblD type
(0)
Homocystinuria without methylmalonic aciduria
(0)
Hypocalcemic rickets
(0)
Imerslund-Grasbeck syndrome
(0)
Imerslund-Grasbeck syndrome type 1
(0)
Imerslund-Grasbeck syndrome type 2
(0)
Intrinsic factor and r binder, combined congenital deficiency of
(0)