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About:
http://dbpedia.org/resource/Template:Amino_acid_metabolic_pathology
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
16906854
(xsd:integer)
dbo:
wikiPageRevisionID
972727271
(xsd:integer)
dbp:
wikiPageUsesTemplate
dbt
:Navbox
dbt
:Collapsible_option
prov:
wasDerivedFrom
wikipedia-en
:Template:Amino_acid_metabolic_pathology?oldid=972727271&ns=10
is
dbp:
wikiPageUsesTemplate
of
dbr
:Amino_acid_transport_disorder
dbr
:Aminoaciduria
dbr
:Propionic_acidemia
dbr
:Prolidase_deficiency
dbr
:Sarcosinemia
dbr
:Alkaptonuria
dbr
:Homocystinuria
dbr
:Hyperammonemia
dbr
:Beta-ketothiolase_deficiency
dbr
:Cystathioninuria
dbr
:Cystinuria
dbr
:D-Glyceric_acidemia
dbr
:Dopamine_beta_hydroxylase_deficiency
dbr
:Inborn_errors_of_renal_tubular_transport
dbr
:Melanin
dbr
:Saccharopinuria
dbr
:Citrullinemia
dbr
:Branched-chain_keto_acid_dehydrogenase_kinase_deficiency
dbr
:Congenital_disorders_of_amino_acid_metabolism
dbr
:Organic_acidemia
dbr
:Ornithine_translocase_deficiency
dbr
:Fumarase_deficiency
dbr
:Ochronosis
dbr
:Ocular_albinism_type_1
dbr
:Trimethylaminuria
dbr
:2-Hydroxyglutaric_aciduria
dbr
:6-Pyruvoyltetrahydropterin_synthase_deficiency
dbr
:Tyrosinemia
dbr
:Tyrosinemia_type_II
dbr
:Hartnup_disease
dbr
:Hawkinsinuria
dbr
:3-Methylcrotonyl-CoA_carboxylase_deficiency
dbr
:3-Methylglutaconic_aciduria
dbr
:Aminoacylase_1_deficiency
dbr
:3-Hydroxy-3-methylglutaryl-CoA_lyase_deficiency
dbr
:Cystinosis
dbr
:Carbamoyl_phosphate_synthetase_I_deficiency
dbr
:Fanconi_syndrome
dbr
:Glutaric_acidemia_type_2
dbr
:Glutaric_aciduria_type_1
dbr
:Glycine_encephalopathy
dbr
:Histidinemia
dbr
:Isobutyryl-coenzyme_A_dehydrogenase_deficiency
dbr
:Isovaleric_acidemia
dbr
:List_of_ICD-9_codes_240–279:_endocrine...olic_diseases,_and_immunity_disorders
dbr
:2-Methylbutyryl-CoA_dehydrogenase_deficiency
dbr
:Hermansky–Pudlak_syndrome
dbr
:Hyperhomocysteinemia
dbr
:Hyperlysinemia
dbr
:Hypermethioninemia
dbr
:Hyperprolinemia
dbr
:Hypertryptophanemia
dbr
:Hypervalinemia
dbr
:Argininemia
dbr
:Argininosuccinic_aciduria
dbr
:Maple_syrup_urine_disease
dbr
:Phenylketonuria
dbr
:Pipecolic_acidemia
dbr
:Tyrosinemia_type_I
dbr
:Inborn_errors_of_metabolism
dbr
:Methylmalonic_acidemia
dbr
:Methylmalonyl-CoA_mutase_deficiency
dbr
:Brunner_syndrome
dbr
:Ocular_albinism
dbr
:Oculocutaneous_albinism
dbr
:Carnosinemia
dbr
:Urocanic_aciduria
dbr
:Ethylmalonic_encephalopathy
dbr
:Iminoglycinuria
dbr
:Lysinuric_protein_intolerance
dbr
:Ornithine_transcarbamylase_deficiency
dbr
:Oculocerebrorenal_syndrome
dbr
:N-Acetylglutamate_synthase_deficiency
dbr
:Tyrosinemia_type_III
dbr
:Succinic_semialdehyde_dehydrogenase_deficiency
dbr
:Tetrahydrobiopterin_deficiency
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