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lineaire hypopigmentatie en craniofaciale asymmetrie met anomalieën van acra, ogen en hersenen (aandoening)
lineaire hypopigmentatie en craniofaciale asymmetrie met anomalieën van acra, ogen en hersenen
RHOA-gerelateerde mozaïekvorm van ectodermale dysplasie
lineaire hypopigmentatie en craniofaciale asymmetrie met afwijkingen van acra, ogen en hersenen
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
RHOA (ras homolog family member A) related mosaic ectodermal dysplasia
RHOA-related mosaic ectodermal dysplasia
A rare ectodermal dysplasia syndrome with characteristics of linear hypopigmentation and hypotrichosis following the lines of Blaschko, symmetric or asymmetric facial dysmorphism and body asymmetry, in association with ocular, dental and acral anomalies. Reported manifestations include microphthalmia, strabismus, myopia, oligodontia, microdontia, conical teeth, abnormal enamel, brachydactyly, syndactyly and broad first toe, as well as dysmorphic facial features such as downslanting palpebral fissures, broad nasal bridge, malar hypoplasia and microstomia. Brain imaging may show cystic leukoencephalopathy and ventricular dilation.
Id1208985003
StatusPrimitive
Associated morphologydysplasie
Finding sitestructuur van ectoderm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyhypoplasie
Finding sitestructuur van pilus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyhypopigmentatie
Finding sitestructuur van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map589608
SNOMED CT to ICD-10 extended map
TargetQ82.4
RuleTRUE
AdviceALWAYS Q82.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified