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(Q55950244)
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English
familial congenital nasolacrimal duct obstruction
human disease
LACRIMAL DUCT DEFECT
Lacrimal Puncta, Absence of
LACRIMAL DUCT DEFECT; LCDD
LCDD
Nasolacrimal Duct Obstruction
In more languages
default values for all languages
No label defined
No description defined
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
disease
0 references
genetic association
IGSF3
1 reference
stated in
Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction
exact match
http://purl.obolibrary.org/obo/HP_0001092
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001092
http://www.orpha.net/ORDO/Orphanet_141083
0 references
http://www.orpha.net/ORDO/Orphanet_451612
0 references
Identifiers
MeSH descriptor ID
C566703
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
4 August 2018
Mondo ID
MONDO_0007871
C566703
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001092
Human Phenotype Ontology ID
HP:0001092
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001092
ICD-10-CM
Q10.5
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
4 August 2018
Mondo ID
MONDO_0007871
ICD-11 ID (Foundation)
729476309
0 references
ICD-11 ID (MMS)
9A11.8
subject named as
Nasolacrimal duct obstruction
0 references
Mondo ID
MONDO_0007871
0 references
OMIM ID
149700
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
4 August 2018
Mondo ID
MONDO_0007871
Orphanet ID
451612
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
4 August 2018
Mondo ID
MONDO_0007871
UMLS CUI
C1835612
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
4 August 2018
Mondo ID
MONDO_0007871
C0344509
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001092
C1867060
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001092
UniProt disease ID
DI-04319
0 references
Sitelinks
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(0 entries)
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Wikibooks
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Wikinews
(0 entries)
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Wikisource
(0 entries)
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Wikiversity
(0 entries)
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Wikivoyage
(0 entries)
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Wiktionary
(0 entries)
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Multilingual sites
(0 entries)
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