Autosomal dominant hereditary disorder	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Multiple malformation syndrome with limb defect as major feature	Symphalangism
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Symphalangism with multiple anomalies of hands and feet syndrome (disorder)
	Symphalangism with multiple anomalies of hands and feet syndrome
	Learman syndrome Symphalangism with multiple anomalies of hands and feet
	An exceedingly rare syndrome described in one family and with characteristics of proximal symphalangism and multiple hand and feet disorders (syndactyly, clinodactyly, hypoplasia of the thenar and hypothenar eminences and a distinctive dermatoglyphic pattern). There have been no further descriptions in the literature since 1981.
	syndroom van symfalangisme met meervoudige anomalieën van handen en voeten
	syndroom van Learman

Id	732955001
Status	Primitive

Associated morphology	Ankylosis
Finding site	Interphalangeal joint structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q74.8
Rule	TRUE
Advice	ALWAYS Q74.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified