Endocrine Diseases

Related topics on Genetics Home Reference:

• 17-beta hydroxysteroid dehydrogenase 3 deficiency
• 21-hydroxylase deficiency
• 22q11.2 deletion syndrome
• 3-M syndrome
• 46,XX testicular disorder of sex development
• 5-alpha reductase deficiency
• androgen insensitivity syndrome
• autoimmune polyglandular syndrome, type 1
• campomelic dysplasia
• cartilage-hair hypoplasia
• congenital hypothyroidism
• hypochondroplasia
• inherited thyroxine-binding globulin deficiency
• Kallmann syndrome
• Klinefelter syndrome
• McCune-Albright syndrome
• multiple endocrine neoplasia
• pseudoachondroplasia
• SADDAN
• Swyer syndrome
• Turner syndrome
• X-linked adrenal hypoplasia congenita
• X-linked adrenoleukodystrophy

You may also search Genetics Home Reference for "Endocrine Diseases" for additional information.