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726735000: Autosomal recessive amelia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3452314017 Autosomal recessive amelia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3452315016 Autosomal recessive amelia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3452316015 Syndrome with characteristics of absence of the upper limbs and severe underdevelopment of the lower limbs. Minor facial abnormalities (depressed nasal root, upturned nose, infra-orbital creases, prominent cheeks and micrognathia) were also reported. The syndrome has been described in three fetuses born to non-consanguineous parents. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
882501000172118 amélie autosomique récessive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive amelia (disorder) Is a Congenital anomaly of lower limb (disorder) true Inferred relationship Some
Autosomal recessive amelia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive amelia (disorder) Is a Congenital complete absence of upper limb false Inferred relationship Some
Autosomal recessive amelia (disorder) Occurrence Congenital true Inferred relationship Some 2
Autosomal recessive amelia (disorder) Occurrence Congenital true Inferred relationship Some 3
Autosomal recessive amelia (disorder) Associated morphology anomalie du développement false Inferred relationship Some 2
Autosomal recessive amelia (disorder) Finding site Lower limb structure true Inferred relationship Some 2
Autosomal recessive amelia (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 3
Autosomal recessive amelia (disorder) Finding site Entire upper limb false Inferred relationship Some 3
Autosomal recessive amelia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive amelia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Autosomal recessive amelia (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal recessive amelia (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Autosomal recessive amelia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Autosomal recessive amelia (disorder) Is a Congenital deformity of bilateral upper limbs (disorder) false Inferred relationship Some
Autosomal recessive amelia (disorder) Finding site Entire right upper extremity true Inferred relationship Some 1
Autosomal recessive amelia (disorder) Finding site Entire left upper extremity true Inferred relationship Some 3
Autosomal recessive amelia (disorder) Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 1
Autosomal recessive amelia (disorder) Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 3
Autosomal recessive amelia (disorder) Is a Congenital complete absence of bilateral upper limbs (disorder) true Inferred relationship Some
Autosomal recessive amelia (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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