Autosomal recessive hereditary disorder	Cerebellar ataxia	Congenital neurological disorder	Developmental hereditary disorder	Ectodermal dysplasia	Hereditary ataxia	Hereditary disorder of the integument
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Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)
	Cerebellar ataxia and ectodermal dysplasia
	Cerebellar ataxia co-occurrent with ectodermal dysplasia
	A very rare disease, characterized by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates cerebellar atrophy.
	cerebellaire ataxie gelijktijdig met ectodermale dysplasie
	syndroom van cerebellaire ataxie en ectodermale dysplasie

Id	715371006
Status	Primitive

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

Associated morphology	Dysplasia
Finding site	Ectoderm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Finding site	Cerebellar structure
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	G11.1
Rule	TRUE
Advice	ALWAYS G11.1
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q82.4
Rule	TRUE
Advice	ALWAYS Q82.4
Correlation	SNOMED CT source code to target map code correlation not specified