Menstrual irregularities

Symptom Information:

Symptom ID: HPO:0000858
Synonyms:
Menstrual irregularity [HPO:0000858]
Menstrual irregularities [OMIM:Menstrual irregularities]
Menstrual irregularity [OMIM:Menstrual irregularity]
Quality:
Cross references:
OMIM: "Menstrual irregularities" [OMIM:Menstrual irregularities]
OMIM: "Menstrual irregularity" [OMIM:Menstrual irregularity]
Is a (Direct Parents):
HPO         Abnormality of the menstrual cycle
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Abnormality of the menstrual cycle(HPO:0000140)
                Menstrual irregularities(HPO:0000858)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
             Abnormal genital system morphology(HPO:0012243)
                Abnormality of the female genitalia(HPO:0010460)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Menstrual irregularities(HPO:0000858)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Menstrual irregularities(HPO:0000858)
MedDRA:
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Acromegaly (Orphanet:963)
Albright hereditary osteodystrophy (Orphanet:665)
Alström syndrome (Orphanet:64)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Blepharophimosis - epicanthus inversus - ptosis (Orphanet:126)
COCKAYNE SYNDROME A (OMIM:216400)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Familial afibrinogenemia (Orphanet:98880)
Familial isolated pituitary adenoma (Orphanet:314777)
GLUCOCORTICOID RESISTANCE, GENERALIZED (OMIM:615962)
Gestational trophoblastic neoplasm (Orphanet:59305)
Gigantism (Orphanet:99725)
Gray platelet syndrome (Orphanet:721)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hydatidiform mole (Orphanet:99927)
Insulin-resistance syndrome type A (Orphanet:2297)
Invasive mole (Orphanet:99925)
Kallmann syndrome (Orphanet:478)
Klippel-Trénaunay syndrome (Orphanet:90308)
Lassa fever (Orphanet:99824)
Malakoplakia (Orphanet:556)
Marburg hemorrhagic fever (Orphanet:99826)
Morgagni-Stewart-Morel syndrome (Orphanet:77296)
PREMATURE OVARIAN FAILURE 1 (OMIM:311360)
PROLACTIN DEFICIENCY, ISOLATED (OMIM:264110)
Peritoneal cystic mesothelioma (Orphanet:168816)
Placental site trophoblastic tumor (Orphanet:99928)
Primary lipodystrophy (Orphanet:90970)
Somatotroph adenoma (Orphanet:96256)
Viral hemorrhagic fever (Orphanet:341)
Wiskott-Aldrich syndrome (Orphanet:906)
Yellow fever (Orphanet:99829)