Condition library · 52 conditions
Conditions: 0–9
- 10q26 deletion syndromeClinical Genetics
- 12q14 microdeletion syndromeClinical Genetics
- 15q11-q13 duplication syndromeClinical Genetics
- 15q11.2 microdeletion syndromeClinical Genetics
- 15q13.3 microdeletionClinical Genetics
- 15q24 microdeletionClinical Genetics
- 16p11.2 deletion syndromeClinical Genetics
- 16p11.2 duplicationClinical Genetics
- 16p12.2 microdeletionClinical Genetics
- 17 alpha-hydroxylase/17,20-lyase deficiencyClinical Genetics
- 17-beta hydroxysteroid dehydrogenase 3 deficiencyClinical Genetics
- 17q12 deletion syndromeClinical Genetics
- 17q12 duplicationClinical Genetics
- 17q24.2 microdeletion syndromeClinical Genetics
- 19p13.13 deletion syndromeClinical Genetics
- 1p36 deletion syndromeClinical Genetics
- 1q21.1 microdeletionClinical Genetics
- 1q21.1 microduplicationClinical Genetics
- 2-hydroxyglutaric aciduriaClinical Genetics
- 21-hydroxylase deficiencyClinical Genetics
- 21q22.11q22.12 microdeletion syndromeClinical Genetics
- 22q11.2 deletion syndromeClinical Genetics
- 22q11.2 duplicationClinical Genetics
- 22q13.3 deletion syndromeClinical Genetics
- 2q37 deletion syndromeClinical Genetics
- 3-beta-hydroxysteroid dehydrogenase deficiencyClinical Genetics
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyMetabolic Medicine
- 3-hydroxyacyl-CoA dehydrogenase deficiencyClinical Genetics
- 3-M syndromeOrthopaedics
- 3-methylcrotonyl-CoA carboxylase deficiencyMetabolic Medicine
- 3-methylglutaconyl-CoA hydratase deficiencyMetabolic Medicine
- 3MC syndromeClinical Genetics
- 3p deletion syndromeClinical Genetics
- 3q29 microdeletion syndromeClinical Genetics
- 3q29 microduplication syndromeClinical Genetics
- 46,XX testicular difference of sex developmentClinical Genetics
- 46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiencyClinical Genetics
- 46,XY gonadal dysgenesis-motor and sensory neuropathy syndromeClinical Genetics
- 47,XYY syndromeClinical Genetics
- 48,XXXY syndromeClinical Genetics
- 48,XXYY syndromeClinical Genetics
- 49,XXXXY syndromeClinical Genetics
- 5-alpha reductase deficiencyClinical Genetics
- 5q minus syndromeClinical Genetics
- 5q31.3 microdeletion syndromeClinical Genetics
- 6q terminal deletion syndromeClinical Genetics
- 6q24-related transient neonatal diabetes mellitusDiabetology
- 7q11.23 duplication syndromeClinical Genetics
- 8p11 myeloproliferative syndromeClinical Genetics
- 8q24.3 microdeletion syndromeClinical Genetics
- 9q22.3 microdeletionClinical Genetics
- 9q33.3q34.11 microdeletion syndromeClinical Genetics