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33313004: Radioulnar synostosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
55586011 Radioulnar synostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
764701016 Radioulnar synostosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4498041000241117 synostose radio-ulnaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3418331001000119 Radio-ulnare Synostose, kongenitale 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
Radioulnar synostosis Is a Congenital anomaly of joint false Inferred relationship Some
Radioulnar synostosis Is a Failure of differentiation of bones of forearm false Inferred relationship Some
Radioulnar synostosis Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
Radioulnar synostosis Finding site Synostosis false Inferred relationship Some
Radioulnar synostosis Finding site Bone structure of ulna false Inferred relationship Some 1
Radioulnar synostosis Occurrence Congenital false Inferred relationship Some
Radioulnar synostosis Associated morphology Fusion true Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of proximal ulna false Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of radius false Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of proximal radius false Inferred relationship Some 1
Radioulnar synostosis Associated morphology anomalie du développement false Inferred relationship Some
Radioulnar synostosis Is a Congenital anomaly of radius false Inferred relationship Some
Radioulnar synostosis Is a Congenital anomaly of ulna (disorder) false Inferred relationship Some
Radioulnar synostosis Associated morphology anomalie congénitale false Inferred relationship Some 1
Radioulnar synostosis Is a Congenital abnormal fusion of radius false Inferred relationship Some
Radioulnar synostosis Is a Congenital abnormal fusion of ulna false Inferred relationship Some
Radioulnar synostosis Is a Arthropathy (disorder) false Inferred relationship Some
Radioulnar synostosis Finding site Bone structure of radius false Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of ulna true Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of radius false Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of ulna false Inferred relationship Some 1
Radioulnar synostosis Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
Radioulnar synostosis Is a Disorder of forearm (disorder) true Inferred relationship Some
Radioulnar synostosis Associated morphology anomalie congénitale false Inferred relationship Some 2
Radioulnar synostosis Finding site Bone structure of upper limb (body structure) false Inferred relationship Some 2
Radioulnar synostosis Occurrence Congenital false Inferred relationship Some 3
Radioulnar synostosis Associated morphology anomalie du développement false Inferred relationship Some 3
Radioulnar synostosis Finding site Upper extremity, including shoulder, arm, forearm, wrist, and hand false Inferred relationship Some 3
Radioulnar synostosis Associated morphology Congenital abnormal fusion false Inferred relationship Some 4
Radioulnar synostosis Occurrence Congenital false Inferred relationship Some 4
Radioulnar synostosis Finding site Structure of bone of forearm (body structure) false Inferred relationship Some 4
Radioulnar synostosis Finding site Structure of bone of forearm (body structure) false Inferred relationship Some 1
Radioulnar synostosis Occurrence Congenital false Inferred relationship Some 1
Radioulnar synostosis Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Radioulnar synostosis Finding site Bone structure of radius true Inferred relationship Some 2
Radioulnar synostosis Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
Radioulnar synostosis Occurrence Congenital false Inferred relationship Some 2
Radioulnar synostosis Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Radioulnar synostosis Is a Finding of bone of upper limb true Inferred relationship Some
Radioulnar synostosis Is a Disorder of bone (disorder) true Inferred relationship Some
Radioulnar synostosis Associated morphology Fusion true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Proximal radioulnar synostosis Is a True Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis and dislocation of radial head Is a False Radioulnar synostosis Inferred relationship Some
Distal radioulnar synostosis Is a True Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis-microcephaly-scoliosis syndrome, also known as Guiffré-Tsukahara syndrome, is an extremely rare syndrome characterized by the association of radioulnar synostosis with microcephaly, scoliosis, short stature and intellectual deficit. Is a False Radioulnar synostosis Inferred relationship Some
A rare syndromic craniosynostosis characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism. Is a False Radioulnar synostosis Inferred relationship Some
Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome is characterized by the association of proximal fusion of the radius and ulna with congenital amegakaryocytic thrombocytopenia. Less than 10 cases have been reported in the literature so far. The syndrome is transmitted as an autosomal dominant trait and is caused by mutations in the HOXA11 gene (7p15). Is a False Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis-developmental delay-hypotonia syndrome, also known as Der Kaloustian-McIntosh-Silver syndrome, is an extremely rare syndrome with synostosis described in about 4 patients to date with clinical manifestations including congenital unilateral radioulnar synostosis, generalized hypotonia, developmental delay, and dysmorphic facial features (long face, prominent nose and ears). Is a False Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis of bilateral upper limbs Is a False Radioulnar synostosis Inferred relationship Some
Congenital radioulnar synostosis Is a True Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis following traumatic injury (disorder) Is a True Radioulnar synostosis Inferred relationship Some
Left radioulnar synostosis Is a True Radioulnar synostosis Inferred relationship Some
Radioulnar synostosis of right forearm (disorder) Is a True Radioulnar synostosis Inferred relationship Some

This concept is not in any reference sets

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