111313001: Syndactyly (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

178545018 Syndactyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

187735012 Mule foot en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

187736013 Congenital webbing of digits en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

189321019 Syndactylia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

189322014 Syndactylism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

189323016 Syndactylus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

630229018 Syndactyly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Syndactyly	Is a	Congenital anomaly of limb	false	Inferred relationship	Some
Syndactyly	Finding site	Musculoskeletal structure of limb	false	Inferred relationship	Some
Syndactyly	Associated morphology	Congenital webbing	false	Inferred relationship	Some	1
Syndactyly	Occurrence	Congenital	false	Inferred relationship	Some
Syndactyly	Finding site	Digit structure	false	Inferred relationship	Some	1
Syndactyly	Associated morphology	anomalie du développement	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare congenital malformation characterised by a unilateral, complete or partial, absence of the pectoralis major (and often minor) muscle, ipsilateral breast and nipple anomalies, hypoplasia of the pectoral subcutaneous tissue, absence of pectoral and axillary hair, and possibly accompanied by chest wall and/or upper limb defects.	Is a	False	Syndactyly	Inferred relationship	Some
Apert's syndrome	Is a	False	Syndactyly	Inferred relationship	Some
Acrocephalosyndactyly type V (disorder)	Is a	False	Syndactyly	Inferred relationship	Some
Symphalangy	Is a	False	Syndactyly	Inferred relationship	Some

This concept is not in any reference sets