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1926006: Osteopetrosis (disorder)


Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4322018 Osteopetrosis en Synonym Active Case insensitive SNOMED CT core
747194012 Osteopetrosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteopetrosis Pathological process Pathological developmental process true Inferred relationship Some 1
Osteopetrosis Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Osteopetrosis Has interpretation Below reference range true Inferred relationship Some 2
Osteopetrosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteopetrosis Interprets Osteoclast turnover rate true Inferred relationship Some 2
Osteopetrosis Is a Chronic disease of musculoskeletal system true Inferred relationship Some
Osteopetrosis Clinical course Progressive true Inferred relationship Some 3
Osteopetrosis Is a Developmental hereditary disorder true Inferred relationship Some
Osteopetrosis Associated morphology Congenital anomaly false Inferred relationship Some 1
Osteopetrosis Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Osteopetrosis Finding site Bone structure false Inferred relationship Some 1
Osteopetrosis Associated morphology Congenital anomaly false Inferred relationship Some 1
Osteopetrosis Occurrence Congenital false Inferred relationship Some 2
Osteopetrosis Associated morphology Developmental abnormality false Inferred relationship Some 2
Osteopetrosis Finding site Bone structure false Inferred relationship Some 2
Osteopetrosis Occurrence Congenital true Inferred relationship Some 1
Osteopetrosis Finding site Bone structure true Inferred relationship Some 1
Osteopetrosis Finding site Bone structure false Inferred relationship Some 1
Osteopetrosis Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteopetrosis hypogammaglobulinaemia syndrome Is a False Osteopetrosis Inferred relationship Some
Osteochondrodysplasia with osteopetrosis Is a True Osteopetrosis Inferred relationship Some
Infantile malignant osteopetrosis Is a False Osteopetrosis Inferred relationship Some
Infantile malignant osteopetrosis Is a True Osteopetrosis Inferred relationship Some
Osteopetrosis - delayed type Is a True Osteopetrosis Inferred relationship Some
Benign autosomal dominant osteopetrosis Is a True Osteopetrosis Inferred relationship Some
Osteopetrosis - unclassified Is a False Osteopetrosis Inferred relationship Some
Transient infantile osteopetrosis Is a True Osteopetrosis Inferred relationship Some
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome Is a True Osteopetrosis Inferred relationship Some
Infantile osteopetrosis with neuroaxonal dysplasia syndrome Is a True Osteopetrosis Inferred relationship Some
Autosomal dominant osteopetrosis type 2 Is a True Osteopetrosis Inferred relationship Some
Osteopetrosis - intermediate type Is a True Osteopetrosis Inferred relationship Some
Osteopetrosis with renal tubular acidosis Is a True Osteopetrosis 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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