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237890006: Autosomal dominant hypophosphatemic bone disease (disorder)


Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356515012 Autosomal dominant hypophosphataemic bone disease en Synonym Active Case insensitive SNOMED CT core
356517016 Autosomal dominant hypophosphatemic bone disease en Synonym Active Case insensitive SNOMED CT core
626684018 Autosomal dominant hypophosphatemic bone disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant hypophosphataemic bone disease Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Bone structure false Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Occurrence Congenital false Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Associated morphology Impaired mineralisation false Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Pathological process Pathological developmental process false Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Associated morphology Impaired mineralisation true Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Finding site Bone structure true Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Pathological process Pathological developmental process true Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Due to Specific renal tubule transport defect true Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Is a Lesion of bone true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Developmental hereditary disorder true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Hypophosphataemia true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Specific renal tubule transport defect false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Dysplasia with defective mineralisation true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Hereditary disorder of the urinary system false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Bone structure false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Is a Metabolic bone disease true Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Inherited disorder of connective tissue false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Bone structure false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Due to Specific renal tubule transport defect false Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Associated morphology Congenital dysplasia false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Osteoid tissue false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Osteoid tissue true Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Occurrence Congenital true Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Associated morphology Congenital dysplasia false Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Finding site Osteoid tissue false Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Occurrence Congenital false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Finding site Skeletal system structure false Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Kidney structure false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Associated morphology Dysplasia true Inferred relationship Some 1
Autosomal dominant hypophosphataemic bone disease Finding site Osteoid tissue false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Finding site Cartilaginous tissue structure false Inferred relationship Some
Autosomal dominant hypophosphataemic bone disease Is a Familial x-linked hypophosphataemic vitamin D refractory rickets false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis Is a True Autosomal dominant hypophosphataemic bone disease Inferred relationship Some
Autosomal dominant hypophosphataemic rickets Is a True Autosomal dominant hypophosphataemic bone disease Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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