Diseases

Headache Disorders, Primary

headache disorders, primary

Entity Type: Diseases
Relation Groups: 3
Relation Preview: 24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name: Headache Disorders, Primary
Standard Disease Name: headache disorders, primary
MeSH Tree: No data
ICD-10: Q96|Q96.0|Q96.9

Identifiers

DO ID: No data
MeSH ID: D014424
OMIM ID: No data
UMLS ID: C0041408
HPO ID: No data

Description and Extensions

Description: NCI2016_02D:A gonadal dysgenesis syndrome occurring in phenotypic females, characterized by the complete absence of one of the sex chromosomes. Signs and symptoms include short stature and hypogonadism.|NCI2016_02D:A gonadal dysgenesis syndrome occurring in phenotypic females, characterized by the absence of a part or all of one of the sex chromosomes. Signs and symptoms include short stature, webbing of neck, low-set ears, hypogonadism, and sterility.|MSH2017_2016_08_12:A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant.|MEDLINEPLUS_20151021:Turner syndrome is a genetic disorder that affects a girl's development. The cause is a missing or incomplete X chromosome. Girls who have it are short, and their ovaries don't work properly. Other physical features typical of Turner syndrome are <ul> <li> Short, "webbed" neck with folds of skin from tops of shoulders to sides of neck</li> <li> Low hairline in the back</li> <li> Low-set ears</li> <li> Swollen hands and feet</li> </ul> Most women with Turner syndrome are <a href='https://www.nlm.nih.gov/medlineplus/femaleinfertility.html'>infertile</a>. They are at risk for health difficulties such as high blood pressure, kidney problems, diabetes, cataracts, osteoporosis, and thyroid problems. Doctors diagnose Turner syndrome based on symptoms and a genetic test. Sometimes it is found in prenatal testing. There is no cure for Turner syndrome, but there are some treatments for the symptoms. Growth hormone often helps girls reach heights that are close to average. Hormone replacement can help start sexual development. Assisted reproduction techniques can help some women with Turner syndrome get pregnant. NIH: National Institute of Child Health and Human Development|JABL99:A syndrome in which the affected patients have only 45 chromosomes, the loss of one of the X chromosomes producing an XO chromosome constitution. The syndrome occurs in 1/2500 female births and nearly 99% of XO fetuses are aborted. Gonadal agenesis and short stature are the main features in the surviving infants. Associated anomalies may included webbed neck, cubitus valgus, shield chest, short stature, lymphedema, coarctation of the aorta, pigmented nevi, and various renal, skeletal, dermatologic, neoplastic, and autoimmune complications. Mental retardation is attributed to ring chromosome X. The phenotype varies and not all abnormalities occur in all patients.|CSP2006:genetic disease that produces sterile females due to monosomy for X chromosome; the ovaries are rudimentary or missing; other abnormalities include short stature, webbed neck, and a broad chest with widely spaced nipples.|CHV2011_02:genetic disease that produces sterile females due to the X chromosome defect|CHV2011_02:genetic disease that produces sterile females due to the X chromosome defect|CHV2011_02:genetic disease that produces sterile females due to the X chromosome defect|CHV2011_02:genetic disease that produces sterile females due to the X chromosome defect|CHV2011_02:genetic disease that produces sterile females due to the X chromosome defect

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