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48130008: Hypogonadism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
80201014 Hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
785664015 Hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
80201014 Hypogonadism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
80201014 Hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
785664015 Hypogonadism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
785664015 Hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
404871000172111 hypogonadisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
404871000172111 hypogonadisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

101 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypogonadism (disorder) Is a Disease of the genitourinary system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism (disorder) Is a Disorder of endocrine gonad true Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism (disorder) Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
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
Postablative ovarian failure Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Postablative testicular hypofunction Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
hypogonadisme, diabète sucré, alopécie, arriération mentale et anomalies électrocardiographiques Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ovarian failure Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A disorder of sex development (DSD) characterised by the presence of female external genitalia, ambiguous genitalia or variable defects in virilisation in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS). Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Female hypogonadism syndrome Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadotropic hypogonadism Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Male hypogonadism Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypogonadism Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Secondary ovarian failure Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral atrophy of testes (disorder) Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadal obesity Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantilism (disorder) Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism with anosmia Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Gonad postablative failure Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary hypogonadism (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome is characterized by congenital muscular dystrophy, infantile cataract and hypogonadism. It has been described in seven individuals from an isolated Norwegian village and in one unrelated individual. Transmission appears to be autosomal recessive. Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Boucher Neuhäuser syndrome Is a False Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Deafness and hypogonadism syndrome (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Syndromic X-linked intellectual disability type 7 (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Scholte syndrome Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cataract with deafness and hypogonadism syndrome Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) Is a True Hypogonadism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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