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609520005: Disorder of fetal structure (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Fetal finding\Fetal disorder\Disorder of fetal structure

\Disease\Disorder of foetus and/or newborn\Fetal disorder\Disorder of fetal structure
\Disease\Developmental disorder\Disorder of fetal structure

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2013. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Disorder of fetal structure	Is a	sygdom specificeret iht. lokalisation	false	Inferred relationship	Some
Disorder of fetal structure	Finding site	Fetal structure	false	Inferred relationship	Some	1
Disorder of fetal structure	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	1
Disorder of fetal structure	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Disorder of fetal structure	Is a	Developmental disorder	true	Inferred relationship	Some
Disorder of fetal structure	Occurrence	Fetal period	true	Inferred relationship	Some	1
Disorder of fetal structure	Is a	Fetal disorder	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Stenosis of fetal left atrioventricular (not morphologically mitral) valve	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Stenosis of fetal common atrioventricular valve (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Regurgitation of fetal truncal valve	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Stenosis of fetal truncal valve (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal primidone syndrome	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Narrowing of fetal arterial duct	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Progression of fetal right ventricular outflow tract obstruction	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Progression of fetal left ventricular outflow tract obstruction (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal abdominal wall defect (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal carbamazepine syndrome	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal valproate syndrome	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Long axis of fetal heart deviated to left (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Long axis of fetal heart deviated to right (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Anomaly of fetal ear	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Sirenomelus (disorder)	Is a	False	Disorder of fetal structure	Inferred relationship	Some
Congenital amputation of upper limb	Is a	False	Disorder of fetal structure	Inferred relationship	Some
Fetal sirenomelia	Is a	True	Disorder of fetal structure	Inferred relationship	Some
A malformation syndrome reported in offspring (children and grandchildren) of women exposed to diethylstilbestrol (DES) during pregnancy and is characterised by reproductive tract malformations, decreased fertility and increased risk of developing clear cell carcinoma of the vagina and cervix in young women. Reproductive malformations reported in DES syndrome include small, T-shaped uteri and other uterotubal anomalies that increase the risk of miscarriages in women and epididymal cysts, microphallus, cryptorchidism, or testicular hypoplasia in men. DES, a synthetic nonsteroidal estrogen was widely prescribed from 1940-1970 to prevent miscarriage.	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal mediastinal shift to right (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal mediastinal shift to left (disorder)	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Propylthiouracil embryofetopathy is a rare teratologic disease characterized by variable congenital anomalies resulting from maternal treatment and prenatal exposure to propylthiouracil. Anomalies frequently encountered include ear malformations (e.g. accessory auricle, preauricular sinus/fistula/cyst), urinary system malformations (e.g. isolated unilateral kidney, congenital hydronephrosis), gastrointestinal anomalies (e.g. congenital bands with intestinal malrotation) and cardiac defects (e.g. situs inversus dextrocardia, cardiac outflow tract defects).	Is a	True	Disorder of fetal structure	Inferred relationship	Some
Fetal trimethadione syndrome	Is a	True	Disorder of fetal structure	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
2967194014	Disorder of foetal structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2967223015	Disorder of fetal structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2967287017	Disorder of fetal structure (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4941071000005116	sygdom i struktur af foster	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)