Disease browser and phenotype portal

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MSeqDR-LSDB
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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

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Uterine Diseases (D014591)
..Starting node ..Adenomyosis (D062788)
Child Nodes:
Sister Nodes:
..Adenomyosis (D062788)
..Endometrial Hyperplasia (D004714)
..Endometritis (D004716)
..Hematometra (D006409)
..McKusick Kaufman syndrome (C538159)
..Progesterone Resistance (C564871)
..Pyometra (D055112)
..Uterine Cervical Diseases (D002577) 12
..Uterine Hemorrhage (D014592) 3
..Uterine Inversion (D019687)
..Uterine Neoplasms (D014594) 13
..Uterine Prolapse (D014596)
..Uterine Retroversion (D060725)
..Uterine Rupture (D014597) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

293

Name:

Adenomyosis

Definition:

The extension of endometrial tissue (ENDOMETRIUM) into the MYOMETRIUM. It usually occurs in women in their reproductive years and may result in a diffusely enlarged uterus with ectopic and benign endometrial glands and stroma.

Alternative IDs:

ParentIDs:

MESH:D014591

TreeNumbers:

C13.351.500.852.113

Synonyms:

Adenomyoses

Slim Mappings:

Urogenital disease (female)

Reference:

MedGen: D062788
MeSH: D062788
OMIM: 600458;

Genes:

Phenotypes

1	HP:0001892	Abnormal bleeding
2	HP:0000119	Abnormality of the genitourinary system
3	HP:0100607	Dysmenorrhea

Disease Causing ClinVar Variants