Concept information
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Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
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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
...
Congenital anomaly of limb
Longitudinal deficiency of part of limb (disorder)
Congenital undergrowth of partial lower limb
Longitudinal deficiency of tarsal bone
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Congenital anomaly of limb
Longitudinal deficiency of part of limb (disorder)
Congenital undergrowth of partial lower limb
Longitudinal deficiency of tarsal bone
...
Congenital anomaly of limb
Longitudinal deficiency of part of limb (disorder)
Congenital undergrowth of partial lower limb
Longitudinal deficiency of tarsal bone
...
Congenital anomaly of limb
Longitudinal deficiency of part of limb (disorder)
Congenital undergrowth of partial lower limb
Longitudinal deficiency of tarsal bone
...
Congenital deformity
Longitudinal deficiency of part of limb (disorder)
Congenital undergrowth of partial lower limb
Longitudinal deficiency of tarsal bone
Preferred term
Short tarsus with absence of lower eyelashes syndrome (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
- 367575006
- Tarsal bone
Is a
- 363070008
- 363185004
- 363212003
- 363343008
- Congenital absence of cilia
- Dominant hereditary disorder, NOS
- Longitudinal deficiency of tarsal bone
- Multiple malformation syndrome with facial defects as major feature
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/721075001
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