Secondary amenorrhea

Symptom Information:

Symptom ID: HPO:0000869
Synonyms:
Secondary physiologic amenorrhea (finding) [Orphanet:41810]
Secondary physiologic amenorrhea [Orphanet:41810]
Secondary amenorrhea [OMIM:Secondary amenorrhea]
Precocious menopause/secondary amenorrhea [Orphanet:41810]
Amenorrhea secondary [Orphanet:41810]
Amenorrhoea [MedDRA:10001928]
Absence of menstruation [MedDRA:10001928]
Amenorrhea [MedDRA:10001928]
Amenorrhoea NOS [MedDRA:10001928]
Amenorrhoea post pill [MedDRA:10001928]
Amenorrhoea primary [MedDRA:10001928]
Amenorrhoea secondary [MedDRA:10001928]
Menses lack of [MedDRA:10001928]
Post pill amenorrhoea [MedDRA:10001928]
Primary amenorrhoea [MedDRA:10001928]
Secondary amenorrhoea [MedDRA:10001928]
Secondary amenorrhoea (excl pregnancy) [MedDRA:10001928]
Amenorrhea post pill [MedDRA:10001928]
Amenorrhea primary [MedDRA:10001928]
Amenorrhea secondary [MedDRA:10001928]
Amenorrhea, primary [OMIM:Amenorrhea, primary]
Primary amenorrhea (in a subset of patients) [OMIM:Primary amenorrhea (in a subset of patients)]
Primary amenorrhea (in some patients) [OMIM:Primary amenorrhea (in some patients)]
Secondary amenorrhea (in a subset of patients) [OMIM:Secondary amenorrhea (in a subset of patients)]
Quality:
Cross references:
Orphanet:41810 "Precocious menopause/secondary amenorrhea" [Orphanet:41810]
OMIM: "Secondary amenorrhea" [OMIM:Secondary amenorrhea]
OMIM: "Amenorrhea, primary" [OMIM:Amenorrhea, primary]
OMIM: "Primary amenorrhea (in a subset of patients)" [OMIM:Primary amenorrhea (in a subset of patients)]
OMIM: "Primary amenorrhea (in some patients)" [OMIM:Primary amenorrhea (in some patients)]
OMIM: "Secondary amenorrhea (in a subset of patients)" [OMIM:Secondary amenorrhea (in a subset of patients)]
UMLS:C0232940 "Secondary physiologic amenorrhea" [Orphanet:41810]
Is a (Direct Parents):
MedDRA Menstruation with decreased bleeding
Orphanet Abnormality of the endocrine system
HPO         Amenorrhea
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)
                Amenorrhea(HPO:0000141)
                   Secondary amenorrhea(HPO:0000869)
       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)
                         Amenorrhea(HPO:0000141)
                            Secondary amenorrhea(HPO:0000869)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the menstrual cycle(HPO:0000140)
                         Amenorrhea(HPO:0000141)
                            Secondary amenorrhea(HPO:0000869)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Menstrual cycle and uterine bleeding disorders(MedDRA:10013326)
       Menstruation with decreased bleeding(MedDRA:10027341)
          Secondary amenorrhea(HPO:0000869)
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

46,XX disorder of sex development - skeletal anomalies (Orphanet:2975)
46,XX gonadal dysgenesis (Orphanet:243)
AMENORRHEA-GALACTORRHEA SYNDROME (OMIM:104600)
Alpha heavy-chain disease (Orphanet:100025)
Atypical Mayer-Rokitansky-Küster-Hauser syndrome (Orphanet:247768)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
CACH syndrome (Orphanet:135)
Castleman disease (Orphanet:160)
Classic Mayer-Rokitansky-Küster-Hauser syndrome (Orphanet:247775)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Congenital or early infantile CACH syndrome (Orphanet:157713)
Cree leukoencephalopathy (Orphanet:99854)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
GAPO syndrome (Orphanet:2067)
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA (OMIM:228300)
Hemochromatosis, type 2A (OMIM:602390)
Ichthyosis - intellectual deficit - dwarfism - renal impairment (Orphanet:2278)
Juvenile or adult CACH syndrome (Orphanet:157719)
Late infantile CACH syndrome (Orphanet:157716)
Osteosclerosis - ichthyosis - premature ovarian failure (Orphanet:75325)
Ovarioleukodystrophy (Orphanet:99853)
POEMS syndrome (Orphanet:2905)
PREMATURE OVARIAN FAILURE 5 (OMIM:611548)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 1 (OMIM:233400)
Perrault Syndrome 2 (OMIM:614926)
Perrault Syndrome 3 (OMIM:614129)
Perrault Syndrome 4 (OMIM:615300)
Polyneuropathy - intellectual deficit - acromicria - premature menopause (Orphanet:2928)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Satoyoshi syndrome (Orphanet:3130)
Spondyloepimetaphyseal dysplasia, Pakistani type (Orphanet:93282)
Tetrasomy X (Orphanet:9)
Transketolase deficiency (ORPHA:488618)
Trisomy X (Orphanet:3375)
Turner syndrome (Orphanet:881)
Werner syndrome (Orphanet:902)
Xp22.3 microdeletion syndrome (Orphanet:1643)
Xq27.3q28 duplication syndrome (Orphanet:261483)