FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.22-SNAPSHOT | FHIR Version n/a User: [n/a]

267395000: Adrenogenital disorder (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\Disorder of adrenal gland\Adrenogenital disorder

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Adrenogenital disorder
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Adrenogenital disorder
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Adrenogenital disorder
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Adrenogenital disorder

\Disease\Disorder of body system\Disorder of endocrine system\Disorder of adrenal gland\Adrenogenital disorder
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Disorder of retroperitoneal compartment (disorder)\Disorder of adrenal gland\Adrenogenital disorder

Status: current, Not 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
Adrenogenital disorder	Is a	Disorder of adrenal gland	true	Inferred relationship	Some
Adrenogenital disorder	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Adrenogenital disorder	Finding site	Adrenal structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
hyperplasie corticosurrénale congénitale	Is a	False	Adrenogenital disorder	Inferred relationship	Some
Acquired adrenogenital syndrome	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Congenital adrenal hyperplasia	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Virilizing syndrome of adrenal origin	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Feminizing syndrome of adrenal origin	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Other specified adrenogenital disorder	Is a	False	Adrenogenital disorder	Inferred relationship	Some
Adrenogenital disorder NOS	Is a	False	Adrenogenital disorder	Inferred relationship	Some
[X]Other adrenogenital disorders	Is a	False	Adrenogenital disorder	Inferred relationship	Some
Adrenogenital syndrome NOS	Is a	False	Adrenogenital disorder	Inferred relationship	Some
Other adrenogenital syndrome without mention of salt loss	Is a	False	Adrenogenital disorder	Inferred relationship	Some
Feminisation-adrenogenital syndrome	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Testicular lesion of adrenogenital syndrome	Associated with	False	Adrenogenital disorder	Inferred relationship	Some	1
21-hydroxylase deficiency	Is a	False	Adrenogenital disorder	Inferred relationship	Some
3 beta-Hydroxysteroid dehydrogenase deficiency	Is a	False	Adrenogenital disorder	Inferred relationship	Some
A rare, genetic, endocrine disease characterized by defect in conversion of cortisone to active cortisol, resulting in ACTH-mediated excessive androgen release from adrenal glands. Premature adrenarche is typical with precocious pseudopuberty, proportionate tall stature and accelerated bone maturation in males, and hirsutism, oligoamenorrhea, central obesity and infertility in females. Imaging studies may indicate adrenal hyperplasia.	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Generalized glucocorticoid resistance syndrome (disorder)	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Adrenogenital disorder caused by drug (disorder)	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Testicular lesion of adrenogenital syndrome	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Iatrogenic adrenogenital disorder	Is a	True	Adrenogenital disorder	Inferred relationship	Some
Idiopathic adrenogenital disorder	Is a	True	Adrenogenital disorder	Inferred relationship	Some
A rare genetic disease characterized by pre- and postnatal growth restriction, developmental delay, adrenal hypoplasia, genital abnormalities (such as microphallus, hypospadias, or cryptorchidism), thrombocytopenia and/or anemia, recurrent severe invasive infections, and enteropathy with chronic diarrhea. Myelodysplastic syndrome and dysmorphic features (including downslanting palpebral fissures, low-set and posteriorly rotated ears, anteverted nares, camptodactyly, and arachnodactyly, among others) may also be observed.	Is a	True	Adrenogenital disorder	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
398804012	Adrenogenital disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
398805013	Adrenogenital syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
398806014	Androgenital syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
660006013	Adrenogenital disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5107001000241114	affection adrénogénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module