Concept information
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Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
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Genetic disease
Hereditary disease
Inborn error of metabolism
Premature aging syndrome (disorder)
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Skin AND/OR mucosa finding (finding)
Skin finding
Disease of skin
Premature aging syndrome (disorder)
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with facial defects as major feature
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with facial defects as major feature
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Disorder of mandible
Mandibular jaw size anomaly
Hypoplasia of mandibular bone (disorder)
Congenital micrognathism
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Disorder of mandible
Mandibular jaw size anomaly
Hypoplasia of mandibular bone (disorder)
Congenital micrognathism
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Disorder of mandible
Mandibular jaw size anomaly
Hypoplasia of mandibular bone (disorder)
Congenital micrognathism
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Congenital anomaly of head
Congenital abnormality of skull and face bones
Craniofacial microsomia
Congenital micrognathism
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Congenital anomaly of head
Congenital abnormality of skull and face bones
Craniofacial microsomia
Congenital micrognathism
Preferred term
MDP (mandibular hypoplasia, deafness, progeroid) syndrome
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
Interprets
Is a
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/773406003
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