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720575002: Braddock syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of trunk structure\Finding of upper trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Finding of trunk structure\Finding of upper trunk\Finding of region of thorax\Pulmonary artery finding\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Finding of trunk structure\Finding of upper trunk\Finding of region of thorax\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Finding of trunk structure\Disorder of trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Braddock syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Braddock syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Braddock syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Braddock syndrome
\Disease\Disorder of body system\Cardiovascular disease\Cardiovascular system hereditary disorder\Braddock syndrome
\Disease\Disorder of body system\Cardiovascular disease\Vascular disorder\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Disease\Disorder of body system\Cardiovascular disease\Vascular disorder\Disorder of artery\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Disease\Disorder of trunk\Disorder of thoracic segment of trunk\Disorder of thorax\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Braddock syndrome
\Disease\Disorder of soft tissue\Vascular disorder\Disorder of blood vessels of thorax\Disorder of pulmonary circulation\Pulmonary hypertension\Precapillary pulmonary hypertension\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Disease\Disorder of soft tissue\Vascular disorder\Disorder of artery\Pulmonary arterial hypertension\Heritable pulmonary arterial hypertension\Braddock syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Braddock syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Braddock syndrome

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3321296017 Braddock syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

3321297014 Braddock syndrome en Synonym Active Case sensitive SNOMED CT core

3321298016 VATER-like syndrome with pulmonary hypertension, abnormal ear and growth deficiency en Synonym Active Case sensitive SNOMED CT core

3321299012 A rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, with characteristics of VATER-like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Braddock syndrome	Finding site	Pulmonary artery structure	true	Inferred relationship	Some	1
Braddock syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Braddock syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	2
Braddock syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	2
Braddock syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Braddock syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Some
Braddock syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Braddock syndrome	Is a	Cardiovascular system hereditary disorder	true	Inferred relationship	Some
Braddock syndrome	Is a	Heritable pulmonary arterial hypertension	true	Inferred relationship	Some
Braddock syndrome	Finding site	Pulmonary artery structure	false	Inferred relationship	Some
Braddock syndrome	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	2
Braddock syndrome	Occurrence	Congenital	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3321296017	Braddock syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3321297014	Braddock syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3321298016	VATER-like syndrome with pulmonary hypertension, abnormal ear and growth deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
3321299012	A rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, with characteristics of VATER-like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.	en	Definition	Active	Case sensitive	SNOMED CT core