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About:
Fukuyama congenital muscular dystrophy
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An Entity of Type :
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Type:
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New Facet based on Instances of this Class
Attributes
Values
label
fukuyama congenital muscular dystrophy
COEXISTS_WITH
Walker-Warburg congenital muscular dystrophy
Autosome Disorders
schema:identifier
c0410174
ISA
Disease
Hereditary Diseases
Congenital Abnormality
Muscular Dystrophies
CAUSES
Disease
Muscular Dystrophies
Death, Sudden
PROCESS_OF
C0030705
Family
Human
Child
Girls
Boys
sibling
AFFECTS
C0030705
Family
NEG_PROCESS_OF
C0030705
young adulthood
is
LOCATION_OF
of
Brain
Eye
Buttocks
9q31
is
COEXISTS_WITH
of
Pathogenesis
Functional disorder
Hypoplasia
Epilepsy
Muscular Dystrophies
Congenital muscular dystrophy
Congenital anomaly of brain
Radiologic finding
Severe Mental Retardation
Lissencephaly
Myopathy, Central Core
Impairment, intellectual
HMN (Hereditary Motor Neuropathy) Proximal Type I
Microgyria
is
ASSOCIATED_WITH
of
genetic locus
Cessation of life
DNA Sequence
alpha-Dystroglycan
Dystonia
Phenotype
Genotype
is
DIAGNOSES
of
Assay
Muscle biopsy
Magnetic Resonance Imaging
Autopsy
Microscopy
Light microscopy
is
CAUSES
of
Genes
Mutation
Fibrosis
Implantation procedure
Equine laminitis
FKTN
is
TREATS
of
Implantation procedure
Fusion procedure
Anesthetics
Surgical repair
Brain natriuretic peptide
Surgical Procedures, Elective
Total intravenous anesthesia
Scoliosis surgery
Posterior spinal instrumentation
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