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English
Johnson–Munson syndrome
rare syndrome
Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome
Johnson-Munson syndrome
APHALANGY WITH HEMIVERTEBRAE
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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_0008806
class of disease
0 references
subclass of
syndrome with limb reduction defects
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
dysostosis of genetic origin with limb anomaly as a major feature
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
exact match
http://www.orpha.net/ORDO/Orphanet_1112
0 references
Identifiers
MeSH descriptor ID
C535881
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
ICD-10-CM
Q87.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
Mondo ID
MONDO_0008806
0 references
OMIM ID
207620
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
Orphanet ID
1112
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
UMLS CUI
C1859754
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0008806
Sitelinks
Wikipedia
(1 entry)
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enwiki
Johnson–Munson syndrome
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Multilingual sites
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