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(Q30990102)
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English
hypogonadotropic hypogonadism
hypogonadism characterized by a impaired signalling by gonadotrpin relasing hormone
isolated congenital gonadotropin deficiency
congenital idiopathic hypogonadotropic hypogonadism
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
hypogonadism
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0090070
hypogonadotropism
0 references
genetic association
FGFR1
1 reference
stated in
The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
on focus list of Wikimedia project
WikiProject Medicine
0 references
NCI Thesaurus ID
C113347
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0090070
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0090070
http://identifiers.org/doid/DOID:0090070
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
KEGG ID
H00255
0 references
Disease Ontology ID
DOID:0090070
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0090070
ICD-10-CM
E23.0
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0090070
Orphanet ID
432
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0090070
478
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0090070
UMLS CUI
C5680088
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
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