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732955001: Symphalangism with multiple anomalies of hands and feet syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498437014 Symphalangism with multiple anomalies of hands and feet en Synonym Active Case insensitive SNOMED CT core
3498438016 Symphalangism with multiple anomalies of hands and feet syndrome en Synonym Active Case insensitive SNOMED CT core
3498439012 Learman syndrome en Synonym Active Case sensitive SNOMED CT core
3498440014 Symphalangism with multiple anomalies of hands and feet syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3499923019 An exceedingly rare syndrome described in one family and with characteristics of proximal symphalangism and multiple hand and feet disorders (syndactyly, clinodactyly, hypoplasia of the thenar and hypothenar eminences and a distinctive dermatoglyphic pattern). There have been no further descriptions in the literature since 1981. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Symphalangism with multiple anomalies of hands and feet Pathological process Pathological developmental process true Inferred relationship Some 1
Symphalangism with multiple anomalies of hands and feet Associated morphology Ankylosis true Inferred relationship Some 1
Symphalangism with multiple anomalies of hands and feet Is a Developmental hereditary disorder true Inferred relationship Some
Symphalangism with multiple anomalies of hands and feet Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Symphalangism with multiple anomalies of hands and feet Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Symphalangism with multiple anomalies of hands and feet Is a Symphalangism true Inferred relationship Some
Symphalangism with multiple anomalies of hands and feet Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Symphalangism with multiple anomalies of hands and feet Associated morphology Congenital ankylosis false Inferred relationship Some 1
Symphalangism with multiple anomalies of hands and feet Occurrence Congenital true Inferred relationship Some 1
Symphalangism with multiple anomalies of hands and feet Finding site Interphalangeal joint structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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