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(Q55781386)
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English
polydactyly of a biphalangeal thumb
No description defined
Thumb Polydactyly
POLYDACTYLY, PREAXIAL I
Fromont Anomaly
Polydactyly, Preaxial type 1
Preaxial polydactyly type 1
PPD1
Thenar Hypoplasia
In more languages
default values for all languages
No label defined
No description defined
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Statements
instance of
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
class of disease
0 references
subclass of
thumb duplication
0 references
exact match
http://purl.obolibrary.org/obo/HP_0001177
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001177
http://www.orpha.net/ORDO/Orphanet_93339
0 references
Identifiers
MeSH descriptor ID
C536332
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
C536332
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001177
Human Phenotype Ontology ID
HP:0001177
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001177
ICD-10-CM
Q69.1
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
Mondo ID
MONDO_0008269
0 references
OMIM ID
174400
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
Orphanet ID
93339
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
UMLS CUI
C1868116
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
C1846474
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
C1395852
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008269
C1395852
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0001177
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