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267395000: Adrenogenital disorder (disorder)


Status: current, Not 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
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
1611271000005112 adrenogenital sygdom da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


38 descendants. Search Descendants:

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
Kongenit adrenal kortikal hyperplasi Is a False Adrenogenital disorder Inferred relationship Some
Acquired adrenogenital syndrome (disorder) 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
Anden specificeret adrenogenital sygdom Is a False Adrenogenital disorder Inferred relationship Some
Adrenogenital sygdom, ikke nærmere specificeret Is a False Adrenogenital disorder Inferred relationship Some
[X]Other adrenogenital disorders Is a False Adrenogenital disorder Inferred relationship Some
adrenogenitalt syndrom, ikke nærmere specificeret Is a False Adrenogenital disorder Inferred relationship Some
andet adrenogenitalt syndrom uden angivelse af salttab 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 with characteristics of a 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

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