Akinesia	Autosomal recessive hereditary disorder	Congenital anomaly of skeletal muscle	Hereditary disorder of musculoskeletal system	Hereditary myopathy	Inherited arthrogryposis
\|	\|	\|	\|	\|	\|

Fetal akinesia, cerebral and retinal hemorrhage syndrome (disorder)
	Lethal congenital contracture syndrome type 5
	Fetal akinesia, cerebral and retinal hemorrhage syndrome
	A rare lethal congenital myopathy syndrome characterized by decreased fetal movements and polyhydramnios in utero and the presence of akinesia, severe hypotonia with respiratory insufficiency, absent reflexes, joint contractures, skeletal abnormalities with thin ribs and bones, intracranial and retinal hemorrhages and decreased birth weight in the neonate.
	syndroom van foetale akinesie, cerebrale bloeding en retinale bloeding
	LCCS5 letaal congenitaal contractuursyndroom type 5

Id	763346009
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Skeletal muscle structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Contracture
Finding site	Structure of joint region
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Decreased
Interprets	Range of joint movement

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G71.2
Rule	TRUE
Advice	ALWAYS G71.2 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified