Oligomenorrhea

Symptom Information:

Symptom ID: HPO:0000876
Synonyms:
oligomenorrhea [HPO:0000876]
Oligomenorrhea [OMIM:Oligomenorrhea]
Oligomenorrhea (in some patients) [OMIM:Oligomenorrhea (in some patients)]
Quality:
Cross references:
OMIM: "Oligomenorrhea" [OMIM:Oligomenorrhea]
OMIM: "Oligomenorrhea (in some patients)" [OMIM:Oligomenorrhea (in some patients)]
UMLS:C2057730 "oligomenorrhea" [HPO:0000876]
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)
                Oligomenorrhea(HPO:0000876)
       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)
                         Oligomenorrhea(HPO:0000876)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Oligomenorrhea(HPO:0000876)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Cerebellar ataxia - hypogonadism (Orphanet:1173)
Cortisone reductase deficiency 1 (OMIM:604931)
Cushing disease (Orphanet:96253)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
GORDON HOLMES SYNDROME (OMIM:212840)
HYPERPROLACTINEMIA (OMIM:615555)
Hyperandrogenism due to cortisone reductase deficiency (Orphanet:168588)
POLYCYSTIC OVARY SYNDROME 1 (OMIM:184700)
Perrault Syndrome 4 (OMIM:615300)
Prader-Willi syndrome (Orphanet:739)
Wolfram syndrome 2 (OMIM:604928)