A severe form of congenital adrenal hyperplasia characterized by very low or absent activity of an enzyme in the steroidogenic pathway typically presenting early in life, and requiring life-long cortisol replacement.
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congenital lipoid adrenal hyperplasia due to STAR deficency
MONDO:0008725
congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
MONDO:0008727
classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
MONDO:0008728
congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
MONDO:0008729
congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
MONDO:0008730
congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
MONDO:0013310