Glycogen storage disease type IX
Glycogen storage disease type IX is a hereditary deficiency of glycogen phosphorylase kinase B that affects the liver and skeletal muscle tissue. It is inherited in an X-linked or autosomal recessive manner.
primaryTopic
Glycogen storage disease type IX
Glycogen storage disease type IX is a hereditary deficiency of glycogen phosphorylase kinase B that affects the liver and skeletal muscle tissue. It is inherited in an X-linked or autosomal recessive manner.
has abstract
Glycogen storage disease type ...... or autosomal recessive manner.
@en
geneReviewsId
geneReviewsName
Phosphorylase Kinase Deficiency
@en
ICD10
medical cause
medical diagnosis
OMIM id
symptoms
Link from a Wikipage to an external page
Wikipage page ID
17,107,820
page length (characters) of wiki page
Wikipage revision ID
982,725,995
Link from a Wikipage to another Wikipage
caption
Glycogen structure
@en
causes
Mutations in PHKA1, PHKA2, PHKB, or PHKG2 genes
@en
diagnosis
CBC, Urinalysis
@en
GeneReviewsName
Phosphorylase Kinase Deficiency
@en
GeneReviewsNBK
ICD
@en
E74.09
@en
name
Glycogen storage disease IX
@en
OMIM
symptoms
Enlarged liver
@en
treatment
Physical therapy, follow metabolic nutritionist
@en
wikiPageUsesTemplate
wordnet_type
hypernym
comment
Glycogen storage disease type ...... or autosomal recessive manner.
@en
label
Glycogen storage disease type IX
@en
wasDerivedFrom
isPrimaryTopicOf
name
Glycogen storage disease IX
@en