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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
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virtrdf-ifp
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None
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About:
Denys-Drash Syndrome
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An Entity of Type :
about:dsyn#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
dsyn
New Facet based on Instances of this Class
Attributes
Values
label
denys-drash syndrome
COEXISTS_WITH
Rare Diseases
Nephroblastoma
Hernia, Diaphragmatic
ASSOCIATED_WITH
Point Mutation
schema:identifier
c0950121
ISA
Disease
Kidney Diseases
Syndrome
Nephroblastoma
Pseudohermaphroditism
CAUSES
Complication
Congenital nephrotic syndrome NOS
PROCESS_OF
C0030705
Child
Adult
Mus
Infant
House mice
Boys
Monozygotic twins
AFFECTS
Sclerosis
NEG_PROCESS_OF
C0030705
MANIFESTATION_OF
Dominant-Negative Mutation
is
LOCATION_OF
of
Kidney
is
COEXISTS_WITH
of
Kidney Diseases
Sclerosis
Nephroblastoma
Nephrosis
Male Pseudohermaphroditism
Pseudohermaphroditism
Frasier Syndrome
is
ASSOCIATED_WITH
of
Tumor Suppressor Genes
WT1 gene|WT1
Predisposition
Genotype
WT1 Protein|WT1
alpha-Fetoproteins
PAX2
is
CAUSES
of
Mutation
WT1 gene|WT1
Dominant-Negative Mutation
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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