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Rule:
asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-eturtle-containers
virtrdf-hashtag
virtrdf-ifp
virtrdf-label
virtrdf-meta-entity-class
None
Inverse Functional Properties:
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"Same As":
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Apply to subjects only
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About:
Blepharophimosis 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
blepharophimosis syndrome
COEXISTS_WITH
Hereditary Diseases
Rare Diseases
schema:identifier
c0265237
ISA
Disease
Congenital Abnormality
Child Development Disorders
Clinical finding
Congenital anomaly of eyelid
PROCESS_OF
C0030705
Family
member
Child
Individual
Woman
Population Group
Brothers
Infant, Newborn
son
Nephew
AFFECTS
Family
PREDISPOSES
Pathogenesis
is
LOCATION_OF
of
Eye
Eyelid structure
Entire eyelid
is
COEXISTS_WITH
of
Disorder of endocrine ovary
Ovarian failure
Ovarian Failure, Premature
ptosis
Female infertility
Trisomy
Menopause, Premature
Ectropion
Eyelid malposition
Telecanthus
is
ASSOCIATED_WITH
of
Genes
3p25
FOXL2
lhcgr
is
CAUSES
of
Genes
Mutation
Germ-Line Mutation
Forkhead Transcription Factors
foxl2
is
TREATS
of
Screening procedure
Excision
Surgical repair
Polypropylene suture
-plasty
is
AFFECTS
of
Gene Mutation
FOXL2
SOX14
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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