Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Mental Disorders (D001523)
..Starting node
..expand
Sexual and Gender Disorders (D019968)

       Child Nodes:
........expandDisorders of Sex Development (D012734) Child107
........expandSexual Dysfunctions, Psychological (D020018) Child14



 Sister Nodes: 
..expandAdjustment Disorders (D000275)
..expandAnxiety Disorders (D001008) Child15
..expandChromosome 18 Pericentric Inversion (C563734)
..expandDelirium, Dementia, Amnestic, Cognitive Disorders (D019965) Child100
..expandDissociative Disorders (D004213) Child1
..expandEating Disorders (D001068) Child6
..expandEpilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505)
..expandFactitious Disorders (D005162) Child3
..expandFragile Site 16p12 (C565001)
..expandHydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
..expandImpulse Control Disorders (D007174) Child4
..expandMental Disorders Diagnosed in Childhood (D019952) Child693
..expandMood Disorders (D019964) Child23
..expandMyoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786)
..expandNeurotic Disorders (D009497)
..expandPersonality Disorders (D010554) Child12
..expandRenal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies (C566918)
..expandSchizophrenia and Disorders with Psychotic Features (D019967) Child15
..expandSexual and Gender Disorders (D019968) Child123
..expandSleep Disorders (D012893) Child41
..expandSomatoform Disorders (D013001) Child4
..expandSpongiform Encephalopathy with Neuropsychiatric Features (C564678)
..expandSubstance-Related Disorders (D019966) Child38
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10164
Name:Sexual and Gender Disorders
Definition:Mental disorders related to sexual dysfunction, paraphilias, and gender identity disorders.
Alternative IDs:
ParentIDs:MESH:D001523
TreeNumbers:F03.800
Synonyms:
Slim Mappings:Mental disorder
Reference: MedGen: D019968
MeSH: D019968
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants