- Autosomal recessive hereditary disorder
- Congenital blepharophimosis
- Congenital esotropia
- Congenital ptosis
- Congenital strabismus
- Hereditary disorder of the visual system
- Multiple malformation syndrome with facial-limb defects as major feature (disorder)
- Short stature disorder (disorder)
- Syndactyly of toes
Name: Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)
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- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
- Frydman Cohen Karmon syndrome
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Concept ID: 717914000- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
- Frydman Cohen Karmon syndrome
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Read Codes:
ICD-10 Codes: Q878