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| category_1_x_health_topic.id | category_1.id | category_1.ts | category_1.title | health_topic.id | health_topic.ts | health_topic.title | health_topic.important | health_topic.general_discussion |
|---|---|---|---|---|---|---|---|---|
| 1 | 1 | 2017-09-20 04:25:34 | a | 1 | 2017-09-20 04:28:54 | A1AT Deficiency | ||
| 2 | 1 | 2017-09-20 04:25:34 | a | 2 | 2017-09-20 04:38:45 | Aarskog Syndrome | It is possible that the main title of the report Aarskog Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Aarskog syndrome is an extremely rare genetic disorder marked by stunted growth that may not become obvious until the child is about three years of age, broad facial abnormalities, musculoskeletal and genital anomalies, and mild intellectual disability. |
| 3 | 1 | 2017-09-20 04:25:34 | a | 3 | 2017-09-20 04:38:49 | Aarskog-Scott Syndrome | It is possible that the main title of the report Aarskog Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Aarskog syndrome is an extremely rare genetic disorder marked by stunted growth that may not become obvious until the child is about three years of age, broad facial abnormalities, musculoskeletal and genital anomalies, and mild intellectual disability. |
| 4 | 1 | 2017-09-20 04:25:34 | a | 4 | 2017-09-20 04:38:51 | AAS | It is possible that the main title of the report Aarskog Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Aarskog syndrome is an extremely rare genetic disorder marked by stunted growth that may not become obvious until the child is about three years of age, broad facial abnormalities, musculoskeletal and genital anomalies, and mild intellectual disability. |
| 5 | 1 | 2017-09-20 04:25:34 | a | 5 | 2017-09-20 04:39:02 | Aase Syndrome | It is possible that the main title of the report Aase Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Aase syndrome is a rare genetic disorder that may be detected during early infancy. The disorder is primarily characterized by the presence of three bones (phalanges) within the thumbs (triphalangeal thumbs) rather than the normal two and abnormally reduc |
| 6 | 1 | 2017-09-20 04:25:34 | a | 6 | 2017-09-20 04:39:06 | Aase-Smith Syndrome II | It is possible that the main title of the report Aase Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Aase syndrome is a rare genetic disorder that may be detected during early infancy. The disorder is primarily characterized by the presence of three bones (phalanges) within the thumbs (triphalangeal thumbs) rather than the normal two and abnormally reduc |
| 7 | 1 | 2017-09-20 04:25:34 | a | 7 | 2017-09-20 04:39:11 | AAT | It is possible that the main title of the report Alpha-1 Antitrypsin Deficiency is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Alpha-1 antitrypsin deficiency (A1AD) is a hereditary disorder characterized by low levels of a protein called alpha-1 antitrypsin (A1AT) which is found in the blood. This deficiency may predispose an individual to several illnesses and most commonly mani |
| 8 | 1 | 2017-09-20 04:25:34 | a | 8 | 2017-09-20 04:39:14 | AAT Deficiency | It is possible that the main title of the report Alpha-1 Antitrypsin Deficiency is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Alpha-1 antitrypsin deficiency (A1AD) is a hereditary disorder characterized by low levels of a protein called alpha-1 antitrypsin (A1AT) which is found in the blood. This deficiency may predispose an individual to several illnesses and most commonly mani |
| 9 | 1 | 2017-09-20 04:25:34 | a | 9 | 2017-09-20 04:39:18 | Abdominal Migraine | It is possible that the main title of the report Cyclic Vomiting Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Cyclic vomiting syndrome (CVS) is a rare disorder characterized by recurrent, similar episodes of severe nausea and vomiting. An episode may last for a few hours to several days and then is followed by a period of time during which affected individuals ar |
| 10 | 1 | 2017-09-20 04:25:34 | a | 10 | 2017-09-20 04:39:24 | Abdominal Muscle Deficiency Syndrome | It is possible that the main title of the report Prune Belly Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Prune-Belly syndrome, also known as Eagle-Barrett syndrome, is a rare disorder characterized by partial or complete absence of the stomach (abdominal) muscles, failure of both testes to descend into the scrotum (bilateral cryptorchidism), and/or urinary t |
| 11 | 1 | 2017-09-20 04:25:34 | a | 11 | 2017-09-20 04:39:25 | Abdominal Wall Defect | It is possible that the main title of the report Gastroschisis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Gastroschisis is a rare congenital disorder in which a defect is present in the wall of the abdomen. Typically there is a small abdominal cavity with herniated abdominal organs that usually appear on the right side of the abdomen. There is no membranous s |
| 12 | 1 | 2017-09-20 04:25:34 | a | 12 | 2017-09-20 04:39:27 | Abercrombie Syndrome | It is possible that the main title of the report Amyloidosis is not the name you expected. | Amyloidosis is a systemic disorder that is classified into several types. The different types of systemic amyloidosis are classified as primary, secondary or familial (hereditary). Primary amyloidosis (also called AL, or ‘light chain') is the most common |
| 13 | 1 | 2017-09-20 04:25:34 | a | 13 | 2017-09-20 04:39:36 | Abetalipoproteinemia | It is possible that the main title of the report Abetalipoproteinemia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Summary Abetalipoproteinemia is a rare inherited disorder of/affecting fat metabolism. Abnormalities in fat metabolism result in malabsorption of dietary fat and various essential vitamins. Affected individuals experience progressive neurological deterior |
| 14 | 1 | 2017-09-20 04:25:34 | a | 14 | 2017-09-20 04:39:39 | Abiotrophic Ophthalmoplegia Externa | It is possible that the main title of the report Congenital Fibrosis of the Extraocular Muscles is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Congenital fibrosis of the extraocular muscles (CFEOM) includes at least five rare genetic eye movement disorders present at birth that are characterized by incomitant strabismus. Specifically, there is an inability to move the eyes in certain directions |
| 15 | 1 | 2017-09-20 04:25:34 | a | 15 | 2017-09-20 04:39:48 | ABL | It is possible that the main title of the report Abetalipoproteinemia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Summary Abetalipoproteinemia is a rare inherited disorder of/affecting fat metabolism. Abnormalities in fat metabolism result in malabsorption of dietary fat and various essential vitamins. Affected individuals experience progressive neurological deterior |
| 16 | 1 | 2017-09-20 04:25:34 | a | 16 | 2017-09-20 04:39:57 | Ablepharon Macrostomia Syndrome | It is possible that the main title of the report Ablepharon-Macrostomia Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Ablepharon-Macrostomia Syndrome (AMS) is an extremely rare inherited disorder characterized by various physical abnormalities affecting the head and facial (craniofacial) area, the skin, the fingers, and the genitals. In addition, affected individuals may |
| 17 | 1 | 2017-09-20 04:25:34 | a | 17 | 2017-09-20 04:28:54 | Abnormal Pap Test | ||
| 18 | 1 | 2017-09-20 04:25:34 | a | 18 | 2017-09-20 04:28:54 | Abortion | ||
| 19 | 1 | 2017-09-20 04:25:34 | a | 19 | 2017-09-20 04:28:54 | Abruptio Placenta | ||
| 20 | 1 | 2017-09-20 04:25:34 | a | 20 | 2017-09-20 04:28:54 | Abruption, Placental | ||
| 21 | 1 | 2017-09-20 04:25:34 | a | 21 | 2017-09-20 04:40:29 | ABS -- Amniotic Bands | It is possible that the main title of the report Amniotic Band Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Amniotic band syndrome is a well-known condition potentially associated with a variety of different birth defects. It is important to note that no two cases of amniotic band syndrome are exactly alike and that the associated symptoms are highly variable. |
| 22 | 1 | 2017-09-20 04:25:34 | a | 22 | 2017-09-20 04:40:45 | ABS -- Antley Bixler Syndrome | It is possible that the main title of the report Antley Bixler Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Antley-Bixler Syndrome is a rare genetic disorder that is primarily characterized by distinctive malformations of the head and facial (craniofacial) area and additional skeletal abnormalities. For example, the disorder is typically associated with prematu |
| 23 | 1 | 2017-09-20 04:25:34 | a | 23 | 2017-09-20 04:28:54 | Abscessed Tooth | ||
| 24 | 1 | 2017-09-20 04:25:34 | a | 24 | 2017-09-20 04:41:07 | Absence Defect of Limbs, Scalp and Skull | It is possible that the main title of the report Adams Oliver Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Adams-Oliver syndrome (AOS) is an extremely rare inherited disorder characterized by defects of the scalp and abnormalities of the fingers, toes, arms, and/or legs. The physical abnormalities associated with this disorder vary greatly among affected indiv |
| 25 | 1 | 2017-09-20 04:25:34 | a | 25 | 2017-09-20 04:28:54 | Absence of Menstruation, Primary | ||
| 26 | 1 | 2017-09-20 04:25:34 | a | 26 | 2017-09-20 04:28:54 | Absence Seizure | ||
| 27 | 1 | 2017-09-20 04:25:34 | a | 27 | 2017-09-20 04:41:26 | Abt-Letterer-Siwe Disease | It is possible that the main title of the report Langerhans Cell Histiocytosis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Langerhans cell histiocytosis (LCH) is a spectrum of rare disorders characterized by overproduction (proliferation) and accumulation of a specific type of white blood cell (histiocyte) in the various tissues and organs of the body (lesions). The lesions m |
| 28 | 1 | 2017-09-20 04:25:34 | a | 28 | 2017-09-20 04:28:54 | Abuse, Child | ||
| 29 | 1 | 2017-09-20 04:25:34 | a | 29 | 2017-09-20 04:41:43 | ACADL | It is possible that the main title of the report Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD) is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) is a rare genetic disorder of fatty acid metabolism that is transmitted as an autosomal recessive trait. It occurs when an enzyme needed to break down certain very long-chain fatty acids is missing |
| 30 | 1 | 2017-09-20 04:25:34 | a | 30 | 2017-09-20 04:41:51 | ACADM Deficiency | It is possible that the main title of the report Medium Chain Acyl CoA Dehydrogenase Deficiency is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. | Medium chain acyl-CoA dehydrogenase (MCAD) deficiency is a rare genetic metabolic disorder characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase. This enzyme is found to be most active in the liver, certain white blood cells (leu |
| category_1_x_health_topic.id | category_1.id | category_1.ts | category_1.title | health_topic.id | health_topic.ts | health_topic.title | health_topic.important | health_topic.general_discussion |