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59451000: Cutis laxa, autosomal recessive (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

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


7 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Cutis laxa, recessive, type I Is a True Cutis laxa, autosomal recessive Inferred relationship Existential restriction modifier
Cutis laxa, recessive, type II Is a True Cutis laxa, autosomal recessive Inferred relationship Existential restriction modifier
Macrocephaly, alopecia, cutis laxa, scoliosis syndrome Is a True Cutis laxa, autosomal recessive Inferred relationship Existential restriction modifier
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Is a True Cutis laxa, autosomal recessive Inferred relationship Existential restriction modifier
Cutis laxa-corneal clouding-oligophrenia syndrome Is a True Cutis laxa, autosomal recessive Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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