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205681004: Gonadal dysgenesis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315432016 Gonadal dysgenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591083017 Gonadal dysgenesis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4886361000241113 dysgénésie gonadique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


120 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gonadal dysgenesis Is a Disorder of endocrine gonad false Inferred relationship Some
Gonadal dysgenesis Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Gonadal dysgenesis Finding site Gonadal endocrine structure false Inferred relationship Some
Gonadal dysgenesis Associated morphology anomalie congénitale du développement false Inferred relationship Some 1
Gonadal dysgenesis Finding site Gonadal structure false Inferred relationship Some 1
Gonadal dysgenesis Is a Disorder of reproductive system false Inferred relationship Some
Gonadal dysgenesis Is a Genital finding false Inferred relationship Some
Gonadal dysgenesis Associated morphology anomalie congénitale du développement false Inferred relationship Some 1
Gonadal dysgenesis Finding site Gonadal structure true Inferred relationship Some 1
Gonadal dysgenesis Occurrence Congenital false Inferred relationship Some 2
Gonadal dysgenesis Associated morphology anomalie du développement false Inferred relationship Some 2
Gonadal dysgenesis Finding site Gonadal structure false Inferred relationship Some 2
Gonadal dysgenesis Is a Congenital malformation of genital organs true Inferred relationship Some
Gonadal dysgenesis Occurrence Congenital true Inferred relationship Some 1
Gonadal dysgenesis Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Gonadal dysgenesis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Mixed gonadal dysgenesis Is a True Gonadal dysgenesis Inferred relationship Some
Other gonadal dysgenesis phenotype NOS Is a False Gonadal dysgenesis Inferred relationship Some
Gonadal dysgenesis NOS Is a False Gonadal dysgenesis Inferred relationship Some
Ovarian dysgenesis Is a False Gonadal dysgenesis Inferred relationship Some
Testicular regression syndrome Is a False Gonadal dysgenesis Inferred relationship Some
Congenital anomaly of ovary Is a True Gonadal dysgenesis Inferred relationship Some
Pure gonadal dysgenesis Is a True Gonadal dysgenesis Inferred relationship Some
Congenital anomaly of testis (disorder) Is a True Gonadal dysgenesis Inferred relationship Some
Congenital anomaly of endocrine gonad (disorder) Is a True Gonadal dysgenesis Inferred relationship Some
Congenital absence of gonads Is a True Gonadal dysgenesis Inferred relationship Some
Congenital hypoplasia of gonad Is a True Gonadal dysgenesis Inferred relationship Some
Accessory gonad Is a True Gonadal dysgenesis Inferred relationship Some
A rare syndrome described and characterized by prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions. Is a True Gonadal dysgenesis Inferred relationship Some
PAGOD syndrome is a severe developmental syndrome characterized by multiple congenital anomalies including cardiovascular defects, pulmonary hypoplasia, diaphragmatic defects and genital anomalies. Is a True Gonadal dysgenesis Inferred relationship Some
Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome is characterised by sex reversal in males with a 46, XX (SRY-negative) karyotype, palmoplantar hyperkeratosis and a predisposition to squamous cell carcinoma. To date, five cases (four of whom were brothers) have been described. The aetiology is unknown. Is a True Gonadal dysgenesis Inferred relationship Some
SERKAL (SEx Reversion, Kidneys, Adrenal and Lung dysgenesis) syndrome is characterized by female to male sex reversal and developmental anomalies of the kidneys, adrenal glands and lungs. Is a True Gonadal dysgenesis Inferred relationship Some
Splenogonadal fusion Is a True Gonadal dysgenesis Inferred relationship Some
Male pseudohermaphroditism Is a False Gonadal dysgenesis Inferred relationship Some
Störung der Geschlechtsentwicklung 46,XX, ovotestikuläre Is a False Gonadal dysgenesis Inferred relationship Some
Micro syndrome is an autosomal recessive disorder characterized by ocular and neurodevelopmental defects and by micro genitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism. Is a True Gonadal dysgenesis Inferred relationship Some
46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome is a rare, genetic, developmental defect during embryogenesis disorder characterized by partial (unilateral testis, persistence of Müllerian duct structures) or complete (streak gonads only) gonadal dysgenesis, usually manifesting with primary amenorrhea in individuals with female phenotype but 46,XY karyotype, and sensorimotor dysmyelinating minifascicular polyneuropathy, which presents with numbness, weakness, exercise-induced muscle cramps, sensory disturbances and reduced/absent deep tendon reflexes. Germ cell tumors (seminoma, dysgerminoma, gonadoblastoma) may develop from the gonadal tissue. Is a True Gonadal dysgenesis Inferred relationship Some

This concept is not in any reference sets

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