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Symptoms » Ovary symptoms » Glossary
 

Glossary for Ovary symptoms

Medical terms related to Ovary symptoms or mentioned in this section include:

  • 46,XX testicular DSD: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • 46,XX testicular disorder of sex development: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • Abdominal symptoms: Symptoms affecting the abdomen or digestive tract
  • Acute oophoritis:
  • Adnexal tenderness: Tenderness of the appendages or secondary structures of the uterus.
  • Adrenoleukodystrophy: A rare hereditary metabolic disease that only occurs in male children and is characterized by adrenal atrophy and extensive cerebral demyelination causing progressive loss of mental functioning, aphasia, apraxia and sometimes blindness. The patient usually dies within 5 years.
  • Ahumada-Del Castillo Syndrome: A form of secondary amenorrhea often resulting from a pituitary gland tumor. The condition causes galactorrhea and amenorrhea even when the patient is not pregnant.
  • Androgen Insensitivity Syndrome: Females with male XY genetics but inability to respond to testosterone.
  • Autoimmune oophoritis: An autoimmune condition where the body's own immune system attacks the ovaries and causes them to become inflamed. It can lead to ovarian function stopping prematurely.
  • Bardet-Biedl syndrome, type 1: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 1 is caused by a defect in chromosome 11q13.
  • Bardet-Biedl syndrome, type 10: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 10 is caused by a defect in chromosome 12q.
  • Bardet-Biedl syndrome, type 11: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 11 is caused by a defect in chromosome 9q33.1.
  • Bardet-Biedl syndrome, type 12: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 12 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 2: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 2 is caused by a defect in chromosome 16q21.
  • Bardet-Biedl syndrome, type 3: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 3 is caused by a defect in chromosome 3p12-q13.
  • Bardet-Biedl syndrome, type 4: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 4 is caused by a defect in chromosome 15q22.3.
  • Bardet-Biedl syndrome, type 5: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 5 is caused by a defect in chromosome 2q31.
  • Bardet-Biedl syndrome, type 6: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 6 is caused by a defect in chromosome 20p12.
  • Bardet-Biedl syndrome, type 7: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 7 is caused by a defect in chromosome 4q27.
  • Bardet-Biedl syndrome, type 8: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 8 is caused by a defect in chromosome 14q32.11.
  • Bardet-Biedl syndrome, type 9: A rare genetic disorder characterized by mental retardation, obesity, polydactyly and retinal pigmentation as well as other abnormalities. Type 9 is caused by a defect in chromosome 7p14.
  • Benign ovarian cyst:
  • Biemond syndrome type 2: A rare inherited condition characterized by mental retardation, obesity, polydactyly and underdeveloped genitals.
  • Bilateral adnexal tenderness: grave gynaecological complication
  • Boucher-Neuhauser syndrome: A very rare disorder characterized by spinocerebellar ataxia, eye abnormalities and a failure of the pituitary to stimulate gonadal development during puberty.
  • Breast tenderness: A feeling of tenderness located anatomically in the breast
  • Cardiomyopathy, hypogonadism, collagenoma syndrome: A rare inherited condition characterized primarily by skin nodules. The skin nodules may be associated with organ system involvement resulting in a variety of other symptoms.
  • Cephalothoracic progressive lipodystrophy: A rare acquired disorder that involves adipose tissue abnormalities and is characterized by loss of adipose tissue mainly in the trunk and arms.
  • Chiari-Frommel syndrome: A hormonal disorder where a woman continues to produce milk even after the child has been weaned.
  • Chudley syndrome 1: A rare syndrome characterized by mental retardation, obesity, hypogonadism and a distinctive mouth.
  • Congenital adrenal hyperplasia -- non-classical form: A late onset form of congenital adrenal hyperplasia where insufficient adrenal corticosteroids are produced by the body due to the deficiency of a particular chemical. The severity of symptoms varies from person to person and onset may occur as early as childhood.
  • Corpus luteum hematoma: Corpus luteum hematoma is a collection of blood in a woman's ovary.
  • De la Chapelle syndrome: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.
  • Deafness hypogonadism syndrome: A rare condition characterized by the combination of hypogonadism and deafness.
  • Dermoid cyst: Benign cystic tumor often containing skin, hair, and other tissue
  • Digestive symptoms: Any symptoms affecting the digestive tract.
  • Disorders of the ovaries:
  • Dup (2) (pter-p13)): A rare chromosomal disorder characterized by various anomalies. The listed symptoms are those observed in the few reported cases. The manifestations linked to most genetic defects are often variable to some degree though early death is quite common.
  • Dysfunctional Uterine Bleeding: Uterus bleeding unrelated to periods
  • Dystrophia myotonica 1: A rare genetic disorder characterized by myotonia, muscle atrophy, cataracts and hypogonadism.
  • Endometriosis: Misplaced uterus tissue causing scar tissue.
  • Enlarged ovaries: Where the ovaries of a female have increased in size to what is considered normal
  • Enlarged ovary: An enlargement of the female ovary to a size bigger than considered normal
  • Fallopian tube symptoms: Symptoms affecting the female fallopian tubes
  • Fatigue: Excessive tiredness or weakness.
  • Female genital organ tumors: Tumors affecting the female genital organs, whether cancerous or bening.
  • Female genital symptoms: Symptoms affecting the female genital organs.
  • Female reproductive symptoms: Symptoms affecting the female reproductive organs.
  • Female sexual symptoms: Symptoms of the female sexual organs.
  • Fertility symptoms: Fertility problems for men or women.
  • Flatulence: Gas passed from the anus
  • Forbes-Albright syndrome: A rare condition where a hormone secreting pituitary or hypothalamic tumor causes galactorrhea and amenorrhea.
  • Fowler-Christmas-Chapple syndrome: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
  • Fragile-X Syndrome: A rare inherited characterized by various physical anomalies as well as mental retardation. The symptoms are milder in females.
  • Fraser-like syndrome: A very rare syndrome characterized by fused eyelids, airway anomalies, cysts in the ovaries and finger and toe abnormalities.
  • GAPO syndrome: A rare condition characterized by retarded growth, alopecia, otpic atrophy and failure of teeth to erupt.
  • Galactorrhea: This is where there is an excessive or spontaneous flow of milk from the female breast
  • Genital symptoms: Symptoms affecting the sex organs.
  • Gigantism: Gigantism refers to abnormally high linear growth due to excessive action of insulin-like growth factor-I (IGF-I) while the epiphyseal growth plates are open during childhood.
  • Headache: Pain affecting the head or brain area.
  • Hirsutism in polycystic ovarian disease: Hirsutism in polycystic ovarian disease is a condition in which there is an excessive growth of dark hair in unusual places on a female's body, such as on the face, that is caused by polycystic ovarian disease.
  • Ichthyosis male hypogonadism: A very rare syndrome characterized mainly by scaly skin and insufficient hormone production by the male gonads.
  • Infertility: Inability of couples to establish pregnancy by having sexual intercourse over a period of time, usually more than 1 year in length.
  • Inflammatory pelvic pain: Inflammatory pelvic pain can be chr, cyclic,non cyclic, localized of generalized, or a combination. It affects women of reproductive age and older. It's important to note that sudden, severe pain with mass indicates a serious disorder such as an ectopic pregnancy, and it also requires immediate evaluation and treatment.
  • Intercourse symptoms: Symptoms related to the act of sexual intercourse.
  • Kallmann Syndrome: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance.
  • Kallmann Syndrome 5: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity may be somewhat variable. Type 5 is linked to a defect on chromosome 8q12.1.
  • Kallmann Syndrome 6: A rare inherited condition characterized by hypogonadism, eunuchoidism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. The symptoms and their severity may be somewhat variable. Type 6 is linked to a defect on chromosome 10q24.
  • Kallmann syndrome 2: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 2 is caused by a genetic defect located at chromosome 8p11.2-p11.1.
  • Kallmann syndrome, type 1, X-linked: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 1 is caused by a genetic defect located at chromosome Xp22.3.
  • Kallmann syndrome, type 3, recessive: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 3 is recessively inherited and the genetic defect is located at chromosome 20p13.
  • Kallmann syndrome, type 4: A rare inherited condition characterized by hypogonadism and impaired or absent sense of smell. The condition occurs as a result of failure of a part of the hypothalamus which results in hormonal imbalance. Type 4 is caused by a genetic defect located at chromosome 3p21.1.
  • Laurence-Moon Syndrome: A rare inherited disorder characterized by vision loss, impaired hormone production, mental retardation and spastic paraplegia.
  • Lower abdominal symptoms: Symptoms affecting the lower abdominal region.
  • Lundberg II syndrome: A rare syndrome involving cataracts, reduced hormone production by ovaries or testes and myopathy which mainly involves the facial and muscles close to the trunk.
  • Martsolf syndrome: A rare inherited condition characterized by mental retardation, cataracts, small head and hypogonadism (reduced production of hormones by ovaries or testes).
  • McCune-Albright Syndrome: A rare genetic multisystem disorder characterized by abnormal skin pigmentation and endocrine gland dysfunction and replacement of parts of bone tissue with fibrous material.
  • Mens health symptoms: Symptoms closely related to men's health.
  • Menstrual irregularities: Various abnormalities of periods and menstruation.
  • Moynahan syndrome I: A rare disorder characterized mainly by multiple moles, underdeveloped genitals, short stature, mental deficiency and heart defect. The moles cover virtually the whole body.
  • Mumps: An acute viral disease that causes the salivary glands to become swollen, sore and inflamed. Immunization had greatly reduced the incidence of this disease.
  • OHSS: Excessive stimulation of the ovaries that usually occurs as a complication of in vitro fertilization but may also occur spontaneously. The degree of excessive ovarian stimulation may vary from mild to severe.
  • Oophoritis: Oophoritis, also known as pelvic inflammatory disease, is an inflammation and infection of a woman's ovaries, often due to a sexually transmitted disease.
  • Ovarian cancer: A condition which is characterized by a malignancy that is located in the ovary
  • Ovarian cyst: A cyst which is located in the ovary
  • Ovarian cysts: Cysts which are located in the ovaries
  • Ovarian tumour: A tumour that is located on the ovary.
  • Ovary conditions: Any condition that affects a female ovary
  • Ovary symptoms: Symptoms affecting the ovaries
  • Pituitary cancer, childhood: Cancer (malignant) of the pituitary gland in children. The pituitary gland produces various hormones and some pituitary tumors (functioning tumors) can affect the secretion of one or more of these hormones resulting in a range of symptoms depending on the exact location of the tumor. Some pituitary tumors do not affect hormone production (nonfunctioning tumors).
  • Polycystic ovarian disease, familial: A rare familial condition characterized by menstrual abnormalities, excessive growth of hair, obesity and infertility.
  • Polycystic ovaries urethral sphincter dysfunction: A rare syndrome characterized by the association of polycystic ovaries with the abnormal functioning of the urinary valve.
  • Polycystic ovary syndrome: Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women.
  • Pregnancy symptoms: Symptoms related to pregnancy.
  • Retinitis pigmentosa, deafness, mental retardation, hypogonadism: A rare genetic disorder characterized by mental retardation, reduced hormone production by the testes or ovaries, deafness and vision problems.
  • Rud Syndrome: A condition characterized by ichthyosis, epilepsy, short stature, hypogonadism and severe mental retardation.
  • Sexual symptoms: Symptoms affecting the sexual organs
  • Tender, fixed adenexal mass: common gynaecological complication
  • Underdeveloped ovaries:
  • Uterus symptoms: Symptoms affecting the female uterus
  • Vaginal symptoms: Symptoms related to the vagina
  • Vohwinkel syndrome: A rare condition where tight bands of thickened skin form around the base of fingers and toes and generally leads to self-amputation of the digit. Hearing loss is also associated with the condition.
  • Vulva symptoms: Symptoms related to the vulva (external skin region near vagina)
  • Weight gain: Gain of body weight.
  • Werner syndrome: A form of premature aging where sufferers start aging during adolescence or soon after and appear old by the time they reach their 30's or 40's. Milder forms of the condition may also occur.
  • Women's health symptoms: Symptoms related to women's health.
  • XX male syndrome: A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY.

Conditions listing medical symptoms: Ovary symptoms:

The following list of conditions have 'Ovary symptoms' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Ovary symptoms:

The following list of medical conditions have 'Ovary symptoms' or similar listed as a medical complication in our database.

 

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