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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
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virtrdf-hashtag
virtrdf-ifp
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None
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About:
Metaphyseal chondrodysplasia
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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
metaphyseal chondrodysplasia
COEXISTS_WITH
Autosome Disorders
Leukoencephalopathy
Metaphyseal chondrodysplasia, McKusick type
schema:identifier
c0265290
ISA
Disease
Chondrodysplasia, unspecified
Osteochondrodysplasias
PART_OF
Mus
PROCESS_OF
C0030705
Family
Human
Boys
sibling
parent
PREDISPOSES
Dysmyelopoietic Syndromes
leukemia
is
LOCATION_OF
of
hair
is
COEXISTS_WITH
of
Hypoplasia
Molecular Pathology
Short stature
Agranulocytosis
Madelung's Neck
SKELETAL DEFORMITY
is
ASSOCIATED_WITH
of
Vision
Immunity, Cellular
Collagen Type X
pth
is
ISA
of
Metaphyseal chondrodysplasia, McKusick type
is
CAUSES
of
Mutation
Valine
Mutation, Missense
COL10A1
is
TREATS
of
pth
is
AFFECTS
of
DNA
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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