Premature ovarian failure

Symptom Information:

Symptom ID: HPO:0008209
Synonyms:
Premature ovarian failure [OMIM:Premature ovarian failure]
Ovarian failure, premature [OMIM:Ovarian failure, premature]
Premature ovarian failure (in a subset of patients) [OMIM:Premature ovarian failure (in a subset of patients)]
Premature ovarian failure (less common) [OMIM:Premature ovarian failure (less common)]
Quality:
Cross references:
OMIM: "Premature ovarian failure" [OMIM:Premature ovarian failure]
OMIM: "Ovarian failure, premature" [OMIM:Ovarian failure, premature]
OMIM: "Premature ovarian failure (in a subset of patients)" [OMIM:Premature ovarian failure (in a subset of patients)]
OMIM: "Premature ovarian failure (less common)" [OMIM:Premature ovarian failure (less common)]
Is a (Direct Parents):
HPO         Abnormality of the ovary
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)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of female internal genitalia(HPO:0000008)
                      Abnormality of the ovary(HPO:0000137)
                         Premature ovarian failure(HPO:0008209)
                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)
MedDRA:
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)