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722459008: syndroom van hypergonadotroop hypogonadisme, verstandelijke beperking en skeletafwijking bij man (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3332220011 Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332226017 Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3332227014 Sohval Soffer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6841971000146110 syndroom van Sohval-Soffer nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7796681000146118 syndroom van hypergonadotroop hypogonadisme, verstandelijke beperking en skeletafwijking bij man nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7796691000146116 syndroom van hypergonadotroop hypogonadisme, verstandelijke beperking en skeletafwijking bij man (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7796701000146116 syndroom van hypergonadotroop hypogonadisme, mentale retardatie en skeletafwijking bij man nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7796711000146119 syndroom van hypergonadotroop hypogonadisme, verstandelijke handicap en skeletafwijking bij man nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3332228016 This syndrome has characteristics of hypergonadotropic hypogonadism, intellectual deficit, and congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. It has been described in two brothers. Testicular biopsy revealed germinal aplasia and complete seminiferous tubular fibrosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a mentale retardatie false Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a X-linked hereditary disease true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Reproductive system hereditary disorder true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Primary testicular failure (disorder) true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Finding site Testicular endocrine structure false Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Has definitional manifestation Decreased hormone production false Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Finding site Bone structure true Inferred relationship Some 3
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Finding site Testicular endocrine structure true Inferred relationship Some 1
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Has interpretation Decreased true Inferred relationship Some 2
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Interprets Hormone production true Inferred relationship Some 2
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 4
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 4
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 5
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) Is a Congenital hypergonadotropic hypogonadism (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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