Premature ovarian failure
Symptom Information:
Symptom ID: | HPO:0008209 | ||||
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 ovary(HPO:0000137) Premature ovarian failure(HPO:0008209) Abnormal internal genitalia(HPO:0000812) Abnormality of female internal genitalia(HPO:0000008) Abnormality of the ovary(HPO:0000137) Premature ovarian failure(HPO:0008209) MedDRA: |
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Database Frequency: | 28 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
CACH syndrome | (Orphanet:135) |
Classic galactosemia | (Orphanet:79239) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type | (Orphanet:363444) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE | (OMIM:615889) |
OVARIAN DYSGENESIS 2 | (OMIM:300510) |
PREMATURE OVARIAN FAILURE 1 | (OMIM:311360) |
PREMATURE OVARIAN FAILURE 2A | (OMIM:300511) |
PREMATURE OVARIAN FAILURE 2B | (OMIM:300604) |
PREMATURE OVARIAN FAILURE 3 | (OMIM:608996) |
PREMATURE OVARIAN FAILURE 5 | (OMIM:611548) |
PREMATURE OVARIAN FAILURE 6 | (OMIM:612310) |
PREMATURE OVARIAN FAILURE 7 | (OMIM:612964) |
PREMATURE OVARIAN FAILURE 8 | (OMIM:615723) |
PREMATURE OVARIAN FAILURE 9 | (OMIM:615724) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |
Perrault Syndrome | (Orphanet:2855) |
Perrault Syndrome 1 | (OMIM:233400) |
Perrault Syndrome 2 | (OMIM:614926) |
Perrault Syndrome 3 | (OMIM:614129) |
Perrault Syndrome 4 | (OMIM:615300) |
Perrault Syndrome 5 | (OMIM:616138) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |