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Code System Concept

Code System Concept Code	717975006
Code System Concept Name	Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder)
Code System Preferred Concept Name	Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	07/31/2016
SDO Date Created	07/31/2016
SDO Date Revised	07/31/2016
Description	A form of autosomal dominant optic atrophy with characteristics of progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance.
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
3310751019	Autosomal dominant optic atrophy and peripheral neuropathy syndrome	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1
Disease	10 , 9 , 8 , 7
Problem Value Set	3

Parent Concepts Parent Concepts Parent/Child (Relationship Type) Dominant hereditary optic atrophy (disorder) {2065009 , SNOMED-CT } Peripheral nerve disease (disorder) {302226006 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts No child concepts present.