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http://www.w3.org/2002/07/owl#
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About:
Cri-du-Chat Syndrome
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An Entity of Type :
about:cgab#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
dsyn
cgab
New Facet based on Instances of this Class
Attributes
Values
label
cri-du-chat syndrome
COEXISTS_WITH
Carrier of disorder
Goldenhar Syndrome
Short arm
schema:identifier
c0010314
ISA
Disease
Hereditary Diseases
Congenital chromosomal disease
PROCESS_OF
C0030705
Child
Adult
Individual
Mothers
Persons
Infant
Girls
Infant, Newborn
Boys
Adolescent
father
Toddler
Bedouins
is
LOCATION_OF
of
21q
is
COEXISTS_WITH
of
Complication
Hypoplasia
Congenital Abnormality
DELETION
Scoliosis, unspecified
Congenital vertical talus
Irido-corneo-trabecular dysgenesis
is
ASSOCIATED_WITH
of
Genome
mosaicism
karyotype
5p13
is
DIAGNOSES
of
Amniocentesis
genetic analysis
Muscle Hypertonia
is
CAUSES
of
Gene Deletion
DELETION
is
TREATS
of
Screening procedure
Probes
Ligation of patent ductus arteriosus
is
AFFECTS
of
Plain x-ray
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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