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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 ..Parathyroid Diseases (D010279)
Child Nodes:
........Hyperparathyroidism (D006961) 12
........Hypoparathyroidism (D007011) 14
........Parathyroid Neoplasms (D010282) 1
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:	8635
Name:	Parathyroid Diseases
Definition:	Pathological processes of the PARATHYROID GLANDS. They usually manifest as hypersecretion or hyposecretion of PARATHYROID HORMONE that regulates the balance of CALCIUM; PHOSPHORUS; and MAGNESIUM in the body.
Alternative IDs:
ParentIDs:	MESH:D004700
TreeNumbers:	C19.642
Synonyms:	Disease, Parathyroid \|Diseases, Parathyroid \|Disorder, Parathyroid \|Disorders, Parathyroid \|Parathyroid Disease \|Parathyroid Disorder \|Parathyroid Disorders
Slim Mappings:	Endocrine system disease
Reference:	MedGen: D010279 MeSH: D010279 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants