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720458005: Acrorenal syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3320829017 Acrorenal syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3320830010 Acrorenal syndrome en Synonym Active Case insensitive SNOMED CT core
3320831014 Acrorenal syndrome comprises a wide spectrum of congenital malformation disorders with characteristics of the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (for example unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract, abdominal well defects, intestinal atresia and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acrorenal syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Acrorenal syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Acrorenal syndrome Occurrence Congenital true Inferred relationship Some 1
Acrorenal syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Acrorenal syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Acrorenal syndrome Finding site Limb structure true Inferred relationship Some 1
Acrorenal syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Acrorenal syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Acrorenal syndrome Is a Congenital anomaly of the kidney true Inferred relationship Some
Acrorenal syndrome Is a Congenital anomaly of limb true Inferred relationship Some
Acrorenal syndrome Is a Hereditary nephropathy true Inferred relationship Some
Acrorenal syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Acrorenal syndrome Occurrence Congenital true Inferred relationship Some 2
Acrorenal syndrome Finding site Kidney structure true Inferred relationship Some 2
Acrorenal syndrome Associated morphology Developmental abnormality false Inferred relationship Some 3
Acrorenal syndrome Occurrence Congenital false Inferred relationship Some 3
Acrorenal syndrome Finding site Limb structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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