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59451000: Cutis laxa, autosomal recessive (disorder)


Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
798295015 Cutis laxa, autosomal recessive (disorder) en Fully specified name Active Case insensitive SNOMED CT core
98752012 Cutis laxa, autosomal recessive en Synonym Active Case insensitive SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cutis laxa, autosomal recessive Pathological process Pathological developmental process true Inferred relationship Some 1
Cutis laxa, autosomal recessive Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Cutis laxa, autosomal recessive Occurrence Congenital true Inferred relationship Some 1
Cutis laxa, autosomal recessive Finding site Connective tissue structure true Inferred relationship Some 1
Cutis laxa, autosomal recessive Associated morphology Congenital anomaly false Inferred relationship Some 1
Cutis laxa, autosomal recessive Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Cutis laxa, autosomal recessive Is a Inherited cutis laxa true Inferred relationship Some
Cutis laxa, autosomal recessive Is a Inherited disorder of connective tissue false Inferred relationship Some
Cutis laxa, autosomal recessive Is a Hereditary disorder of the integument false Inferred relationship Some
Cutis laxa, autosomal recessive Finding site Skin structure false Inferred relationship Some 1
Cutis laxa, autosomal recessive Associated morphology Congenital anomaly false Inferred relationship Some 1
Cutis laxa, autosomal recessive Occurrence Congenital false Inferred relationship Some 2
Cutis laxa, autosomal recessive Associated morphology Developmental abnormality false Inferred relationship Some 2
Cutis laxa, autosomal recessive Finding site Skin structure true Inferred relationship Some 2
Cutis laxa, autosomal recessive Occurrence Congenital false Inferred relationship Some
Cutis laxa, autosomal recessive Finding site Connective tissue structure false Inferred relationship Some
Cutis laxa, autosomal recessive Finding site Structure of musculoskeletal system false Inferred relationship Some
Cutis laxa, autosomal recessive Finding site Skin structure false Inferred relationship Some 1
Cutis laxa, autosomal recessive Finding site Connective tissue false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
RIN2 syndrome Is a True Cutis laxa, autosomal recessive Inferred relationship Some
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Is a True Cutis laxa, autosomal recessive Inferred relationship Some
Cutis laxa-corneal clouding-oligophrenia syndrome Is a True Cutis laxa, autosomal recessive Inferred relationship Some
Cutis laxa, recessive, type I Is a True Cutis laxa, autosomal recessive Inferred relationship Some
Cutis laxa, recessive, type II Is a True Cutis laxa, autosomal recessive Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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