eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital adrenal hyperplasia |
| Symptom | C0268287|steroid 21-hydroxylase deficiency |
| Sentences | 1 |
| PubMedID- 23329749 | Pp is idiopathic (ipp) in most children, but it is the earliest manifestation of non-classical congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency (nc21ohd) in 5%-20% of cases. |
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