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363290007: hereditaire aandoening van voortplantingsstelsel (aandoening)

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

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding (finding)\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Reproductive system hereditary disorder
\Disease\Disorder of body system\Hereditary disorder by system\Reproductive system hereditary disorder
\Disease\Disorder of body system\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of reproductive system\Reproductive system hereditary disorder

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Reproductive system hereditary disorder	Is a	Disorder of reproductive system	true	Inferred relationship	Some
Reproductive system hereditary disorder	Is a	Hereditary disorder by system	true	Inferred relationship	Some
Reproductive system hereditary disorder	Finding site	Structure of anatomical reproductive system (body structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Female infertility due to oocyte meiotic arrest	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Kallman syndrome with heart disease (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
4H leukodystrophy (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
46,XY disorder of sex development due to isolated 17,20-lyase deficiency (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
46,XX ovarian dysgenesis, short stature syndrome (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Congenital leptin deficiency	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Polyendocrine polyneuropathy syndrome (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Robinow syndrome	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Androgen resistance syndrome	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Hereditary malignant epithelial tumor of ovary (disorder)	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some
Hereditary endometrial carcinoma	Is a	True	Reproductive system hereditary disorder	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
482435019	Reproductive system hereditary disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
755097012	Reproductive system hereditary disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6530551000146116	hereditaire aandoening van voortplantingsstelsel	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6530561000146118	erfelijke ziekte van voortplantingssysteem	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6530571000146112	hereditaire aandoening van voortplantingsstelsel (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)