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| health_topic_x_synonyms.id | health_topic.id | health_topic.ts | health_topic.title | health_topic.important | health_topic.general_discussion | synonyms.id | synonyms.ts | synonyms.value |
|---|---|---|---|---|---|---|---|---|
| 1 | 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. | 1 | 2017-09-20 04:38:45 | AAS |
| 2 | 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. | 2 | 2017-09-20 04:38:45 | FGDY |
| 3 | 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 | 2017-09-20 04:38:45 | Aarskog disease |
| 4 | 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. | 4 | 2017-09-20 04:38:45 | Scott Aarskog syndrome |
| 5 | 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. | 5 | 2017-09-20 04:38:45 | Aarskog-Scott syndrome |
| 6 | 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. | 6 | 2017-09-20 04:38:45 | faciodigitogenital syndrome |
| 7 | 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. | 7 | 2017-09-20 04:38:45 | faciogenital dysplasia |
| 8 | 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. | 1 | 2017-09-20 04:38:45 | AAS |
| 9 | 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. | 2 | 2017-09-20 04:38:45 | FGDY |
| 10 | 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. | 3 | 2017-09-20 04:38:45 | Aarskog disease |
| 11 | 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 | 2017-09-20 04:38:45 | Scott Aarskog syndrome |
| 12 | 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. | 5 | 2017-09-20 04:38:45 | Aarskog-Scott syndrome |
| 13 | 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. | 6 | 2017-09-20 04:38:45 | faciodigitogenital syndrome |
| 14 | 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. | 7 | 2017-09-20 04:38:45 | faciogenital dysplasia |
| 15 | 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. | 1 | 2017-09-20 04:38:45 | AAS |
| 16 | 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. | 2 | 2017-09-20 04:38:45 | FGDY |
| 17 | 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. | 3 | 2017-09-20 04:38:45 | Aarskog disease |
| 18 | 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. | 4 | 2017-09-20 04:38:45 | Scott Aarskog syndrome |
| 19 | 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 | 2017-09-20 04:38:45 | Aarskog-Scott syndrome |
| 20 | 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. | 6 | 2017-09-20 04:38:45 | faciodigitogenital syndrome |
| 21 | 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. | 7 | 2017-09-20 04:38:45 | faciogenital dysplasia |
| 22 | 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 | 22 | 2017-09-20 04:39:02 | Aase-Smith Syndrome II |
| 23 | 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 | 23 | 2017-09-20 04:39:02 | Congenital Anemia and Triphalangeal Thumbs |
| 24 | 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 | 24 | 2017-09-20 04:39:02 | Hypoplastic Anemia-Triphalangeal Thumbs, Aase-Smith Type |
| 25 | 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 | 22 | 2017-09-20 04:39:02 | Aase-Smith Syndrome II |
| 26 | 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 | 23 | 2017-09-20 04:39:02 | Congenital Anemia and Triphalangeal Thumbs |
| 27 | 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 | 24 | 2017-09-20 04:39:02 | Hypoplastic Anemia-Triphalangeal Thumbs, Aase-Smith Type |
| 28 | 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 | 28 | 2017-09-20 04:39:11 | A1AD |
| 29 | 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 | 29 | 2017-09-20 04:39:11 | AATD |
| 30 | 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 | 30 | 2017-09-20 04:39:11 | genetic emphysema |
| health_topic_x_synonyms.id | health_topic.id | health_topic.ts | health_topic.title | health_topic.important | health_topic.general_discussion | synonyms.id | synonyms.ts | synonyms.value |