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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 androgeny 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
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2739 | GLO1 | glyoxalase I | |
| 2765 | GML | glycosylphosphatidylinositol anchored molecule like | |
| 3030 | HADHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | |
| 3283 | HSD3B1 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 | |
| 3284 | HSD3B2 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | |
| 3291 | HSD11B2 | hydroxysteroid 11-beta dehydrogenase 2 | |
| 3292 | HSD17B1 | hydroxysteroid 17-beta dehydrogenase 1 | |
| 3293 | HSD17B3 | hydroxysteroid 17-beta dehydrogenase 3 | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 4051 | CYP4F3 | cytochrome P450 family 4 subfamily F member 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P49748 | Very long-chain specific acyl-CoA dehydrogenase, mitochondrial | |
| Q04760 | Lactoylglutathione lyase | |
| Q7LGC8 | Carbohydrate sulfotransferase 3 | |
| Q7RTW8 | Otoancorin |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003251 | Male infertility |
| HP:0003394 | Muscle spasm |
| HP:0004319 | Decreased circulating aldosterone level |
| HP:0004349 | Reduced bone mineral density |
| HP:0008187 | Absence of secondary sex characteristics |
| HP:0008193 | Primary gonadal insufficiency |
| HP:0008197 | Absence of pubertal development |
| HP:0008207 | Primary adrenal insufficiency |
| HP:0008214 | Decreased serum estradiol |
| HP:0008232 | Elevated circulating follicle stimulating hormone level |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 |
| 3284 | HSD3B2 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 |
| 1584 | CYP11B1 | cytochrome P450 family 11 subfamily B member 1 |
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 |
