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About:
http://dbpedia.org/resource/Template:Cytoskeletal_defects
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
29881466
(xsd:integer)
dbo:
wikiPageRevisionID
1067245183
(xsd:integer)
dbp:
wikiPageUsesTemplate
dbt
:Navbox
dbt
:Collapsible_option
prov:
wasDerivedFrom
wikipedia-en
:Template:Cytoskeletal_defects?oldid=1067245183&ns=10
is
dbp:
wikiPageUsesTemplate
of
dbr
:Elejalde_syndrome
dbr
:Epidermolytic_hyperkeratosis
dbr
:MASS_syndrome
dbr
:Hypertrophic_cardiomyopathy
dbr
:Pelger–Huët_anomaly
dbr
:Usher_syndrome
dbr
:Desmin-related_myofibrillar_myopathy
dbr
:Dunnigan_familial_partial_lipodystrophy
dbr
:Emery–Dreifuss_muscular_dystrophy
dbr
:Epidermolysis_bullosa_simplex
dbr
:Gardner's_syndrome
dbr
:Congenital_contractural_arachnodactyly
dbr
:Osteopoikilosis
dbr
:Limb–girdle_muscular_dystrophy
dbr
:Short_rib–polydactyly_syndrome
dbr
:Steatocystoma_multiplex
dbr
:Ichthyosis_bullosa_of_Siemens
dbr
:Keratin_disease
dbr
:May–Hegglin_anomaly
dbr
:Microcephalic_osteodysplastic_primordial_dwarfism_type_II
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:Wiskott–Aldrich_syndrome
dbr
:Laminopathy
dbr
:Tauopathy
dbr
:Alexander_disease
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:Familial_adenomatous_polyposis
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:Barraquer–Simons_syndrome
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:Nonsyndromic_deafness
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:Cavernous_venous_malformation
dbr
:Familial_cirrhosis
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:Hereditary_elliptocytosis
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dbr
:Hereditary_spherocytosis
dbr
:Dilated_cardiomyopathy
dbr
:Arrhythmogenic_cardiomyopathy
dbr
:Asphyxiating_thoracic_dysplasia
dbr
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:Freeman–Sheldon_syndrome
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:Ichthyosis_hystrix
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:Nemaline_myopathy
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:Long_QT_syndrome
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:White_sponge_nevus
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:Terminal_osseous_dysplasia_with_pigmentary_defects
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:Giant_axonal_neuropathy
dbr
:Mandibuloacral_dysplasia
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:Monilethrix
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