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MIRAGE
congenital adrenal hyperplasia
Summary
- Synonym
-
- adrenal hyperplasia 1
- congenital lipoid adrenal hyperplasia
- lipoid CAH
- Definition
- A steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgyny manifestations resulting from steroidogenic enzyme deficiency.
- Super Class
- physical disorder steroid inherited metabolic disorder
External Links
- Disease Ontology
- DOID:0050811
- Mondo Disease Ontology
- UMLS
- ORDO
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1583 | CYP11A1 | cytochrome P450 family 11 subfamily A member 1 | |
| 1584 | CYP11B1 | cytochrome P450 family 11 subfamily B member 1 | |
| 1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 | |
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 | |
| 5447 | POR | cytochrome p450 oxidoreductase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P16435 | NADPH--cytochrome P450 reductase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000953 | Hyperpigmentation of the skin |
| HP:0001007 | Hirsutism |
| HP:0001061 | Acne |
| HP:0001507 | Growth abnormality |
| HP:0001596 | Alopecia |
| HP:0002170 | Intracranial hemorrhage |
| HP:0003154 | Increased circulating ACTH level |
| HP:0004322 | Short stature |
| HP:0005616 | Accelerated skeletal maturation |
| HP:0008236 | Isosexual precocious puberty |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 1584 | CYP11B1 | cytochrome P450 family 11 subfamily B member 1 |
| 1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 |
| 3284 | HSD3B2 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 |
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 |
