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27201004: Acroosteolysis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
45484016 Acroosteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757742011 Acroosteolysis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4477781000241117 acro-ostéolyse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acroosteolysis Is a Degenerative skin disorder false Inferred relationship Some
Acroosteolysis Finding site Skin structure false Inferred relationship Some 1
Acroosteolysis Associated morphology dégénérescence false Inferred relationship Some 1
Acroosteolysis Is a Degenerative skin disorder (disorder) false Inferred relationship Some
Acroosteolysis Associated morphology dégénérescence false Inferred relationship Some 1
Acroosteolysis Finding site Skin structure false Inferred relationship Some 1
Acroosteolysis Is a Disorder of bone (disorder) true Inferred relationship Some
Acroosteolysis Finding site Bone structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Occupational acroosteolysis Is a True Acroosteolysis Inferred relationship Some
Hajdu-Cheney syndrome Is a True Acroosteolysis Inferred relationship Some
Idiopathic acroosteolysis Is a True Acroosteolysis Inferred relationship Some
Giacci familial neurogenic acroosteolysis (disorder) Is a False Acroosteolysis Inferred relationship Some
Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome is an extremely rare ectodermal dysplasia syndrome characterized by hypotrichosis universalis with mild to severe scarring alopecia, acro-osteolysis, onychogryphosis, thin and tapered fingertips, periodontitis and caries leading to premature teeth loss, linear or reticular palmoplantar keratoderma and erythematous, scaling, psoriasis-like skin lesions on arms and legs. Lingua plicata and ventricular tachycardia have also been observed. Is a False Acroosteolysis Inferred relationship Some
A rare, genetic, progeroid syndrome disorder characterized by a prematurely aged appearance (including lipoatrophy, thin, translucent skin, sparse, thin hair, and skeletal muscle atrophy), delayed tooth eruption, keloid-like lesions on pressure regions, and skeletal abnormalities including marked acroosteolysis, brachydactyly with small hands and feet, kyphoscoliosis, osteopenia, and progressive joint contractures in the fingers and toes. Craniofacial features include a thin calvarium, delayed closure of the anterior fontanel, flat occiput, shallow orbits, malar hypoplasia and narrow nose. Is a False Acroosteolysis Inferred relationship Some
Hereditary acroosteolysis (disorder) Is a True Acroosteolysis Inferred relationship Some

This concept is not in any reference sets

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