Not logged in :
Login
Facets (new session)
Description
Metadata
Settings
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:
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects
"Same As":
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects (recommended)
Apply to subjects, objects and predicates (not recommended on big datasets)
Apply to predicates only (special use cases only)
About:
Kallmann Syndrome
Goto
Sponge
NotDistinct
Permalink
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
kallmann syndrome
COEXISTS_WITH
Mental disorders
Infertility
Depressed mood
Congenital heart disease
Anosmia
Hypogonadotropic hypogonadism
Child Development Disorders
Hypogonadism
Prolactinoma
Idiopathic hypogonadotropic hypogonadism
Smelly sensation
ASSOCIATED_WITH
Mutation
Hypogonadotropic hypogonadism
schema:identifier
c0162809
ISA
Disease
Hereditary Diseases
Syndrome
Congenital Abnormality
Anosmia
Hypogonadotropic hypogonadism
Child Development Disorders
Sense of smell impaired
Hypothalamic Diseases
CAUSES
Puberty
Idiopathic hypogonadotropic hypogonadism
PROCESS_OF
C0030705
Family
Human
Child
Adult
Females
Males
Individual
Woman
Population Group
Male population group
cohort
Brothers
Boys
Monozygotic twins
Han Chinese
Twin Multiple Birth
Relative (related person)
Adolescents, Female
Twins, Dizygotic
AFFECTS
Family
Woman
Male population group
NEG_COEXISTS_WITH
Schizophrenia
is
COEXISTS_WITH
of
Pathogenesis
Hypoplasia
loss; bone
Sensorineural Hearing Loss
Histopathology
Anosmia
Hypogonadotropic hypogonadism
Hypesthesia
Neurologic Manifestations
Mirror movements disorder
Klinefelter's Syndrome
Sense of smell impaired
CHROMOSOME REARRANGEMENT
Gene Abnormality
is
ASSOCIATED_WITH
of
Genes
FGF8 gene|FGF8
Gonadorelin|GNRH1
hearing impairment
Pathogenicity
Ability
Ataxia
inorganic phosphate
Anosmia
Magnesium
FGFR1
CHD7
Menstrual cycle
Genotype
FGFR1 gene|FGFR1
CCDC141
ANOS1
PROK2
PRKAR2A|PROKR2
is
DIAGNOSES
of
Magnetic Resonance Imaging
mutation analysis
Stimulation test
is
CAUSES
of
Genes
Mutation
Congenital Abnormality
Gene Mutation
Gonadorelin|GNRH1
Mutation, Missense
CCDC141
ANOS1
Fibroblast Growth Factor Receptor 1
SOX10
EMX2
PROK2 gene|PROK2
KAL1 gene|ANOS1
is
TREATS
of
Diagnosis
◂◂ First
◂ Prev
Next ▸
Last ▸▸
Page 1 of 2
Go
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
About
OpenLink Virtuoso
version 08.03.3322 as of Apr 19 2022, on Linux (x86_64-generic-linux-glibc25), Single-Server Edition (189 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software