Disease Search
Conditions starting from 0 to 9 returned 92 records.
- 10q Partial Trisomy
- 11-Beta-Hydroxylase Deficiency
- 11p partial monosomy syndrome
- 15q13.3 Microdeletion Syndrome
- 16p11.2 deletion syndrome
- 16p11.2 duplication syndrome
- 17-Alpha-Hydroxylase Deficiency
- 17-Beta hydroxysteroid dehydrogenase 3 deficiency
- 17-Beta hydroxysteroid dehydrogenase deficiency
- 17-Beta-Hydroxysteroid Deficiency
- 17-Ketosteroid Reductase Deficiency
- 17p13.1 deletion syndrome
- 17q21.31 Microdeletion Syndrome
- 17q23.1q23.2 Microdeletion Syndrome
- 18 Hydroxylase Deficiency
- 1p partial monosomy
- 1p36 Deletion Syndrome
- 1q21.1 microdeletion syndrome
- 2 Duplication Syndrome
- 2,4-dienoyl-CoA reductase deficiency
- 2,4-Dienoyl-coenzyme A reductase deficiency
- 2-Hydroxyethyl Methacrylate Sensitization
- 2-MBAD deficiency
- 2-MBCD deficiency
- 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (2M3HBA)
- 2-Methylacetoacetyl CoA Thiolase Deficiency
- 2-Methylbutyryl-CoA Dehydrogenase Deficiency
- 2-Methylbutyrylglycinuria
- 2-oxoglutarate complex deficiency
- 21-Hydroxylase Deficiency
- 22q11.2 Deletion Syndrome
- 22q11.2 Duplication Syndrome
- 22q13 Deletion Syndrome
- 22q13.3 Deletion Syndrome
- 2MBG
- 2q37 deletion syndrome
- 3 Methylglutaconic Aciduria Type IV
- 3-Alpha Hydroxyacyl-CoA Dehydrogenase Deficiency
- 3-Beta-Hydroxysteroid Dehydrogenase Deficiency
- 3-Hydroxy-3 Methylglutaryl-CoA Lyase Deficiency (HMG)
- 3-Hydroxy-3-methylglutaric aciduria
- 3-Hydroxyisobutyric Aciduria
- 3-Methylcrotonyl-CoA carboxylase deficiency
- 3-methylglutaconic aciduria
- 3-Methylglutaconic aciduria type 3
- 3-methylglutaconic aciduria type I
- 3-methylglutaconic aciduria type II
- 3-methylglutaconic aciduria type V
- 3-methylglutaconyl-CoA hydratase deficiency
- 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
- 3M syndrome
- 3p deletion syndrome
- 4 alpha aminobutyrate transaminase deficiency
- 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
- 4-enoyl CoA reductase deficiency
- 4-Hydroxyphenylacetic Aciduria
- 4-Hydroxyphenylpyruvate dioxygenase deficiency
- 45, X
- 46, XY disorders of sexual development
- 46,XX Gonadal Dysgenesis Epibulbar Dermoid
- 46,XX sex reversal, type 1
- 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy
- 46,XY sex reversal type 2
- 46,XY sex reversal, type 1
- 46,XY sex reversal, type 3
- 47 XXX Syndrome
- 47, XXX
- 47, XXY
- 47, XXY Female
- 47, XXY Intersex
- 47, XYY
- 47, XYY Syndrome
- 48, XXXX
- 48, XXYY
- 49, XXXXX
- 49, XXXXY
- 49, XXXXY syndrome
- 49,XXXXX Syndrome
- 4p partial monosomy syndrome
- 5-Alpha Reductase Deficiency
- 5-OXO
- 5-Oxoprolinase Deficiency
- 5-Oxoprolinuria
- 5p deletion syndrome
- 5p minus syndrome
- 5p partial monosomy syndrome
- 5p- syndrome
- 5q- Syndrome
- 5q14.3 microdeletion syndrome
- 6 Alpha Mercaptopurine Sensitivity
- 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
- 8p23.1 Duplication Syndrome