syndroom van capillaire malformatie en arterioveneuze malformatie
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RAS p21 protein activator 1-related capillary malformation, arteriovenous malformation (disorder)
RASA1-related capillary malformation, arteriovenous malformation
RAS p21 protein activator 1-related capillary malformation, arteriovenous malformation
CM-AVM1 - capillary malformation-arteriovenous malformation 1
A rare capillary malformation-arteriovenous malformation characterized by single or multiple cutaneous lesions ranging from round to oval shape with pinkish to purplish-red or reddish-brown macules, randomly distributed over the body. Perilesional pale halo is usually detected on the skin. These lesions may occur with or without arteriovenous malformations/arteriovenous fistulas involving muscle, bone, spine and brain. Parkes Weber syndrome with segmental distribution may also be present. Most patients are asymptomatic except for the capillary malformations, the family history is often positive for capillary malformations.
Id1381532005
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van capillair van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetQ27.3
RuleTRUE
AdviceALWAYS Q27.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified