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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Endocrine System Diseases (D004700)
..Starting node ..Gonadal Disorders (D006058)
Child Nodes:
........Disorders of Sex Development (D012734) 107
........Female Athlete Triad Syndrome (D053716)
........Hypogonadism (D007006) 62
........Ovarian Diseases (D010049) 51
........Puberty, Delayed (D011628) 1
........Puberty, Precocious (D011629) 8
........Testicular Diseases (D013733) 28
Sister Nodes:
..ACTH Deficiency, Isolated (C562707)
..Adrenal Gland Diseases (D000307) 71
..Alopecia, Neurologic Defects, and Endocrinopathy Syndrome (C567425)
..Bone Diseases, Endocrine (D001849) 40
..Diabetes Mellitus (D003920) 106
..Dwarfism (D004392) 155
..Endocrine Gland Neoplasms (D004701) 89
..Endocrine-Cerebroosteodysplasia (C567210)
..Gonadal Disorders (D006058) 238
..Macrosomia Adiposa Congenita (C565425)
..Parathyroid Diseases (D010279) 30
..Pituitary Diseases (D010900) 60
..Polyendocrinopathies, Autoimmune (D016884) 4
..Proprotein Convertase 1 3 Deficiency (C563423)
..PROPROTEIN CONVERTASE 1/3 DEFICIENCY (OMIM:600955)
..Retinohepatoendocrinologic Syndrome (C564839)
..Thyroid Diseases (D013959) 92
..Tuberculosis, Endocrine (D014383)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4758
Name:	Gonadal Disorders
Definition:	Pathological processes of the OVARIES or the TESTES.
Alternative IDs:
ParentIDs:	MESH:D004700
TreeNumbers:	C19.391
Synonyms:	Disorder, Gonadal \|Disorders, Gonadal \|Gonadal Disorder
Slim Mappings:	Endocrine system disease
Reference:	MedGen: D006058 MeSH: D006058 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants