dbo:abstract
|
- Tel Hashomer camptodactyly syndrome is a rare genetic disorder which is characterized by camptodactyly,( a condition where one or more fingers or toes are permanently bent), facial dysmorphisms, and fingerprint, skeletal and muscular abnormalities.This disorder is thought to be inherited in an autosomal recessive fashion. (en)
|
dbo:alias
|
- (en)
- Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases. (en)
|
dbo:wikiPageID
| |
dbo:wikiPageLength
|
- 6734 (xsd:nonNegativeInteger)
|
dbo:wikiPageRevisionID
| |
dbo:wikiPageWikiLink
| |
dbp:causes
| |
dbp:diagnosis
|
- Physical evaluation, Radiography (en)
|
dbp:differential
|
- Isolated/idiopathic variant of all of the symptoms (en)
|
dbp:duration
| |
dbp:frequency
|
- Very rare, 23 cases have been reported across the world (en)
|
dbp:name
|
- Tel Hashomer camptodactyly syndrome (en)
|
dbp:onset
| |
dbp:prevention
| |
dbp:prognosis
| |
dbp:specialty
| |
dbp:symptoms
|
- Camptodactyly, facial dysmorphisms, and abnormalities throughout the body (en)
|
dbp:synonyms
|
- Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases. (en)
|
dbp:wikiPageUsesTemplate
| |
dcterms:subject
| |
rdf:type
| |
rdfs:comment
|
- Tel Hashomer camptodactyly syndrome is a rare genetic disorder which is characterized by camptodactyly,( a condition where one or more fingers or toes are permanently bent), facial dysmorphisms, and fingerprint, skeletal and muscular abnormalities.This disorder is thought to be inherited in an autosomal recessive fashion. (en)
|
rdfs:label
|
- Tel Hashomer camptodactyly syndrome (en)
|
owl:sameAs
| |
prov:wasDerivedFrom
| |
foaf:isPrimaryTopicOf
| |
is dbo:wikiPageWikiLink
of | |
is foaf:primaryTopic
of | |