Menorrhagia

Symptom Information:

Symptom ID: HPO:0000132
Synonyms:
Menorrhagia (finding) [Orphanet:40360]
Menostaxis (disorder) [Orphanet:40360]
Menorrhagia [Orphanet:40360]
Menostaxis [Orphanet:40360]
Menorrhagia [OMIM:Menorrhagia]
Metrorrhagia/menorrhagia/hemorrhagic cycles/hyper/poly/spanio/dysmenorrhea [Orphanet:40360]
Menorrhagia [MedDRA:10027313]
Bleeding menstrual heavy [MedDRA:10027313]
Excessive menstruation [MedDRA:10027313]
Excessive or frequent menstruation [MedDRA:10027313]
Heavy periods [MedDRA:10027313]
Hypermenorrhea [MedDRA:10027313]
Hypermenorrhoea [MedDRA:10027313]
Menopausal menorrhagia [MedDRA:10027313]
Menses regular with excessive bleeding [MedDRA:10027313]
Menstrual flooding [MedDRA:10027313]
Menstrual flow excessive [MedDRA:10027313]
Menstruation increased [MedDRA:10027313]
Menstruation prolonged [MedDRA:10027313]
Pre-menopausal menorrhagia [MedDRA:10027313]
Premenopausal menorrhagia [MedDRA:10027313]
Prolonged heavy periods [MedDRA:10027313]
Prolonged menses [MedDRA:10027313]
Prolonged periods [MedDRA:10027313]
Pubertal menorrhagia [MedDRA:10027313]
Menostaxis [MedDRA:10027313]
Menorrhagia (in some patients) [OMIM:Menorrhagia (in some patients)]
Spaniomenorrhea [Orphanet:40360]
Polymenorrhoea [MedDRA:10036086]
Polymenorrhea [Orphanet:40360]
Polymenorrhea (finding) [Orphanet:40360]
Quality:
Cross references:
HPO:0100609 "Hypermenorrhea" [Orphanet:40360]
Orphanet:40360 "Metrorrhagia/menorrhagia/hemorrhagic cycles/hyper/poly/spanio/dysmenorrhea" [Orphanet:40360]
OMIM: "Menorrhagia" [OMIM:Menorrhagia]
OMIM: "Menorrhagia (in some patients)" [OMIM:Menorrhagia (in some patients)]
UMLS:C0025323 "Menorrhagia" [HPO:0000132]
UMLS:C0025323 "Menorrhagia" [Orphanet:40360]
UMLS:C0232966 "Menostaxis" [Orphanet:40360]
UMLS:C0032519 "Polymenorrhea" [Orphanet:40360]
Is a (Direct Parents):
HPO         Abnormality of the menstrual cycle
Orphanet Functional anomalies of the genital system
HPO         Abnormal bleeding
MedDRA Menstruation with increased bleeding
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
             Abnormal genital system morphology(HPO:0012243)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Menorrhagia(HPO:0000132)
                Abnormality of the female genitalia(HPO:0010460)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Menorrhagia(HPO:0000132)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Abnormality of the menstrual cycle(HPO:0000140)
                Menorrhagia(HPO:0000132)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Menorrhagia(HPO:0000132)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Menstrual cycle and uterine bleeding disorders(MedDRA:10013326)
       Menstruation with increased bleeding(MedDRA:10027342)
          Menorrhagia(HPO:0000132)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

BERNARD-SOULIER SYNDROME (OMIM:231200)
BLEEDING DISORDER, PLATELET-TYPE, 12 (OMIM:605735)
BLEEDING DISORDER, PLATELET-TYPE, 19 (OMIM:616176)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bernard-Soulier syndrome (Orphanet:274)
Bleeding diathesis due to glycoprotein VI deficiency (Orphanet:98885)
Congenital factor II deficiency (Orphanet:325)
Congenital factor V deficiency (Orphanet:326)
Congenital factor VII deficiency (Orphanet:327)
Congenital factor X deficiency (Orphanet:328)
Congenital plasminogen activator inhibitor type 1 deficiency (Orphanet:465)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 (OMIM:613625)
FECHTNER SYNDROME (OMIM:153640)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glanzmann thrombasthenia (Orphanet:849)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Gray platelet syndrome (Orphanet:721)
HYPERPROLACTINEMIA (OMIM:615555)
Hermansky-Pudlak syndrome (Orphanet:79430)
INTEGRIN, BETA-3 (OMIM:173470)
MAY-HEGGLIN ANOMALY (OMIM:155100)
PASSOVOY FACTOR DEFECT (OMIM:168830)
PRIMARY RELEASE DISORDER OF PLATELETS (OMIM:176630)
PURPURA SIMPLEX (OMIM:179000)
Quebec platelet disorder (Orphanet:220436)
Von Willebrand disease type 1 (Orphanet:166078)
Von Willebrand disease type 2 (Orphanet:166081)
Von Willebrand disease type 2A (Orphanet:166084)
Von Willebrand disease type 2B (Orphanet:166087)
Von Willebrand disease type 2M (Orphanet:166090)
Von Willebrand disease type 2N (Orphanet:166093)
Von Willebrand disease type 3 (Orphanet:166096)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)