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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-eturtle-containers
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None
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About:
Neonatal hypotonia
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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
neonatal hypotonia
COEXISTS_WITH
Disease
Hereditary Diseases
Syndrome
Obesity
Myopathy
Congenital muscular dystrophy
Paralysed
Prader-Willi Syndrome
Premenstrual syndrome
Neurodevelopmental disorder
Glycogen Storage Disease
FG syndrome
Gillespie syndrome
ASSOCIATED_WITH
Mutation
schema:identifier
c0270971
CAUSES
Ankle stiffness
PROCESS_OF
C0030705
Family
Child
Females
Males
Infant
Brothers
Boys
sibling
Twin Multiple Birth
Twins, Dizygotic
AFFECTS
Motor Development
NEG_PROCESS_OF
Couples
is
LOCATION_OF
of
C0030705
is
COEXISTS_WITH
of
Myopathies, Nemaline
Acidosis, Lactic
Cytochrome-c Oxidase Deficiency
Congenital hypomyelinating neuropathy
is
ASSOCIATED_WITH
of
Pregnancy
Respiratory distress
Muscular stiffness
is
DIAGNOSES
of
Clinicians
Electromyography
is
CAUSES
of
Metabolic Diseases
Bromide poisoning
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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