Menorrhagia
Symptom Information:
Symptom ID: | HPO:0000132 | |||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |