Summary Of: XXXXX syndrome

Encyclodia Page On: XXXXX syndrome

These Are Links To Other Documents

ICD | 10 | Q | DiseasesDB | X chromosomes | karyotyping | microcephaly | micrognathia | palpebral fissures | hypertelorism | strabismus | epicanthus | webbed | Turner's Syndrome | camptodactyly | clinodactyly | talipes equinovarus | Scoliosis | hypotonia | patent ductus arteriosus | atrial septal defect | ventricular septal defect | ovaries | v | Pathology | chromosome abnormalities | Q90-Q99 | 758 | Autosomal | Trisomies | Down syndrome | 21 | Edwards syndrome | 18 | Patau syndrome | 13 | Trisomy 9 | Warkany syndrome 2 | 8 | Trisomy 22 | Cat eye syndrome | 22 | Trisomy 16 | Monosomies | deletions | Wolf-Hirschhorn syndrome | 4 | Cri du chat | 5 | Williams syndrome | 7 | Jacobsen syndrome | 11 | Miller-Dieker syndrome | Smith-Magenis syndrome | 17 | 22q11.2 deletion syndrome | 22 | genomic imprinting | Angelman syndrome | Prader-Willi syndrome | 15 | X | Y | Monosomy | Turner syndrome (XO) | Trisomy | Tetrasomy | other karyotypes | Klinefelter's syndrome (47,XXY) | 48,XXYY | 49,XXXXY | Triple X syndrome (47,XXX) | 48,XXXX | 47,XYY | Translocations | leukemia | lymphoma | Philadelphia chromosome | Burkitt's lymphoma | Anaplastic large cell lymphoma | Follicular lymphoma | Mantle cell lymphoma | Ewing's sarcoma | Gonadal dysgenesis | Mixed gonadal dysgenesis | XX gonadal dysgenesis | Fragile X syndrome | Uniparental disomy | | disease | stub | help | Categories | Diseases | Genetic disorders | Genetics | Disease stubs |