Secondary amenorrhea
Symptom Information:
Symptom ID: | HPO:0000869 | ||||||||||||||||||||||||
Synonyms: |
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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) 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) 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) 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) |
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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) |