Inborn disorder of amino acid transport
MONDO:0019216Also known as: inborn disorder of amino acid absorption and transport, disorder of amino acid absorption and transport
16 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Cystinuria
(7)
Developmental and epileptic encephalopathy, 13
(3)
Oculocerebrorenal syndrome
(3)
Developmental and epileptic encephalopathy, 25
(1)
Developmental and epileptic encephalopathy, 42
(1)
Undetermined early-onset epileptic encephalopathy
(1)
Atypical hypotonia-cystinuria syndrome
(0)
Autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome
(0)
Autosomal recessive spinocerebellar ataxia 13
(0)
Autosomal recessive spinocerebellar ataxia 18
(0)
Blue diaper syndrome
(0)
Cystinuria type A
(0)
Cystinuria type B
(0)
Developmental and epileptic encephalopathy, 21
(0)
Developmental and epileptic encephalopathy, 24
(0)
Developmental and epileptic encephalopathy, 26
(0)
Developmental and epileptic encephalopathy, 28
(0)
Developmental and epileptic encephalopathy, 29
(0)
Developmental and epileptic encephalopathy, 31A
(0)
Developmental and epileptic encephalopathy, 32
(0)
Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Inborn disorder of amino acid metabolism
(6)
Amino acid metabolism disease
(2)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)