363290007: Reproductive system hereditary disorder (disorder)

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:

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
5230361000241117 affection de l'appareil reproducteur, héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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

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This concept is not in any reference sets