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- Guanidinoacetate_methyltransferase_deficiency abstract "Guanidinoacetate methyltransferase deficiency, also called GAMT deficiency, is an autosomal recessive metabolic disorder that primarily affects the nervous system and muscles. It is the first observed disorder of creatine metabolism.".
- Guanidinoacetate_methyltransferase_deficiency diseasesdb "5461".
- Guanidinoacetate_methyltransferase_deficiency omim "601240".
- Guanidinoacetate_methyltransferase_deficiency thumbnail Glycocyamine.png?width=300.
- Guanidinoacetate_methyltransferase_deficiency wikiPageExternalLink condition=guanidinoacetatemethyltransferasedeficiency.
- Guanidinoacetate_methyltransferase_deficiency wikiPageExternalLink NBK3794.
- Guanidinoacetate_methyltransferase_deficiency wikiPageID "12774553".
- Guanidinoacetate_methyltransferase_deficiency wikiPageRevisionID "591523600".
- Guanidinoacetate_methyltransferase_deficiency caption Glycocyamine.
- Guanidinoacetate_methyltransferase_deficiency diseasesdb "5461".
- Guanidinoacetate_methyltransferase_deficiency genereviewsname "Creatine Deficiency Syndromes".
- Guanidinoacetate_methyltransferase_deficiency genereviewsnbk "NBK3794".
- Guanidinoacetate_methyltransferase_deficiency hasPhotoCollection Guanidinoacetate_methyltransferase_deficiency.
- Guanidinoacetate_methyltransferase_deficiency name "Guanidinoacetate methyltransferase deficiency".
- Guanidinoacetate_methyltransferase_deficiency omim "601240".
- Guanidinoacetate_methyltransferase_deficiency wordnet_type synset-disease-noun-1.
- Guanidinoacetate_methyltransferase_deficiency subject Category:Amino_acid_metabolism_disorders.
- Guanidinoacetate_methyltransferase_deficiency subject Category:Autosomal_recessive_disorders.
- Guanidinoacetate_methyltransferase_deficiency subject Category:Rare_diseases.
- Guanidinoacetate_methyltransferase_deficiency type Abstraction100002137.
- Guanidinoacetate_methyltransferase_deficiency type AminoAcidMetabolismDisorders.
- Guanidinoacetate_methyltransferase_deficiency type Attribute100024264.
- Guanidinoacetate_methyltransferase_deficiency type AutosomalRecessiveDisorders.
- Guanidinoacetate_methyltransferase_deficiency type Condition113920835.
- Guanidinoacetate_methyltransferase_deficiency type Disease114070360.
- Guanidinoacetate_methyltransferase_deficiency type Disorder114052403.
- Guanidinoacetate_methyltransferase_deficiency type IllHealth114052046.
- Guanidinoacetate_methyltransferase_deficiency type Illness114061805.
- Guanidinoacetate_methyltransferase_deficiency type PathologicalState114051917.
- Guanidinoacetate_methyltransferase_deficiency type PhysicalCondition114034177.
- Guanidinoacetate_methyltransferase_deficiency type State100024720.
- Guanidinoacetate_methyltransferase_deficiency type Disease.
- Guanidinoacetate_methyltransferase_deficiency type AilmentCondition.
- Guanidinoacetate_methyltransferase_deficiency type Situation.
- Guanidinoacetate_methyltransferase_deficiency comment "Guanidinoacetate methyltransferase deficiency, also called GAMT deficiency, is an autosomal recessive metabolic disorder that primarily affects the nervous system and muscles. It is the first observed disorder of creatine metabolism.".
- Guanidinoacetate_methyltransferase_deficiency label "Guanidinoacetate methyltransferase deficiency".
- Guanidinoacetate_methyltransferase_deficiency sameAs m.02x4cgd.
- Guanidinoacetate_methyltransferase_deficiency sameAs Q5613758.
- Guanidinoacetate_methyltransferase_deficiency sameAs Q5613758.
- Guanidinoacetate_methyltransferase_deficiency sameAs 2427.
- Guanidinoacetate_methyltransferase_deficiency sameAs 434.
- Guanidinoacetate_methyltransferase_deficiency sameAs Guanidinoacetate_methyltransferase_deficiency.
- Guanidinoacetate_methyltransferase_deficiency wasDerivedFrom Guanidinoacetate_methyltransferase_deficiency?oldid=591523600.
- Guanidinoacetate_methyltransferase_deficiency depiction Glycocyamine.png.
- Guanidinoacetate_methyltransferase_deficiency isPrimaryTopicOf Guanidinoacetate_methyltransferase_deficiency.
- Guanidinoacetate_methyltransferase_deficiency name "Guanidinoacetate methyltransferase deficiency".