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41345002: Rickets (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
68966019 Rickets en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
778123018 Rickets (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
952571000195115 rachitismo it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
152701000172110 rachitisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
423251000274116 Rachitis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
460301000274112 Juvenile Osteomalazie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


20 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Rickets Is a Disorder of phosphate, calcium and vitamin D metabolism false Inferred relationship Some
Rickets Is a Disorder with defective osteoid mineralization true Inferred relationship Some
Rickets Finding site Osteoid tissue true Inferred relationship Some 1
Rickets Finding site Cartilaginous tissue structure false Inferred relationship Some
Rickets Is a Functional finding true Inferred relationship Some
Rickets Is a Arthropathy (disorder) true Inferred relationship Some
Rickets Finding site Structure of epiphyseal plate (body structure) true Inferred relationship Some 2
Rickets Interprets Physiologic mineralization of bone true Inferred relationship Some 3
Rickets Has interpretation Deficient true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypophosphatasia rickets Is a True Rickets Inferred relationship Some
Neonatal rickets Is a True Rickets Inferred relationship Some
Rachitic rosary Is a False Rickets Inferred relationship Some
Renal osteodystrophy Is a False Rickets Inferred relationship Some
Glucoaminophosphaturia syndrome with rickets Is a False Rickets Inferred relationship Some
Calcipenic type rickets Is a True Rickets Inferred relationship Some
Phosphopenic type rickets Is a True Rickets Inferred relationship Some
Late effects of rickets (one year OR more) Is a True Rickets Inferred relationship Some
Familial x-linked hypophosphatemic vitamin D refractory rickets Is a True Rickets Inferred relationship Some
Active rickets Is a True Rickets Inferred relationship Some
Celiac rickets Is a True Rickets Inferred relationship Some
Autosomal dominant hypophosphatemic rickets Is a True Rickets Inferred relationship Some
Autosomal recessive hypophosphatemic vitamin D refractory rickets Is a True Rickets Inferred relationship Some
Vitamin D-dependent rickets Is a True Rickets Inferred relationship Some
Rachitic rosary Due to True Rickets Inferred relationship Some 2
à l'examen : chapelet costal Due to False Rickets Inferred relationship Some 3
Rachitic dwarf Due to True Rickets Inferred relationship Some 1
Hypocalcemic rickets (disorder) Is a True Rickets Inferred relationship Some
rachitisme hypophosphatémique autosomique récessif Is a False Rickets Inferred relationship Some
Late effect of rickets After True Rickets Inferred relationship Some 2
A rare hereditary disorder of renal phosphate wasting characterized by hypophosphatemia and hypercalciuria associated with rickets and/or osteomalacia. Other features include slow growth, short stature, skeletal deformities, muscle weakness and bone pain that are associated with normal or elevated plasma levels of calcitriol and hyperphosphaturia. Is a True Rickets Inferred relationship Some

This concept is not in any reference sets

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