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370999003: Primary hypogonadism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1196295012 Primary hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209713018 Primary hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228893011 Hypergonadotropic hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1196295012 Primary hypogonadism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1196295012 Primary hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209713018 Primary hypogonadism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1209713018 Primary hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1228893011 Hypergonadotropic hypogonadism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1228893011 Hypergonadotropic hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5235601000241118 hypogonadisme primaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5235601000241118 hypogonadisme primaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary hypogonadism (disorder) Is a Hypogonadism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypogonadism (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypogonadism (disorder) Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypogonadism (disorder) Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary ovarian failure Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary testicular failure (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked intellectual disability Van Esch type (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked intellectual disability Cilliers type (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hydrocephalus with obesity and hypogonadism syndrome Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism with mitral valve prolapse and intellectual disability syndrome Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare syndromic endocrine disease characterized by the association of hypergonadotropic hypogonadism and cataracts with onset during adolescence. Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder) Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism. Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Woodhouse Sakati syndrome Is a True Primary hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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