Loading disease data
| Disease | Prevalence | Drugs | Proteins | |
|---|---|---|---|---|
| Immunodeficiency 31C (IMD31C) | Ultra-Rare | — | 2 | |
| ACTH-independent macronodular adrenal hyperplasia 1 (AIMAH1) | Ultra-Rare | — | 1 | |
| Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) | N/A | — | 1 | |
| Familial gestational hyperthyroidism (HTFG) | N/A | — | 1 | |
| Growth hormone deficiency, isolated, 3, with agammaglobulinemia (IGHD3) | Uncommon | — | 1 | |
| Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessive (GHISID1) | Ultra-Rare | — | 1 | |
| Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant (GHISID2) | Ultra-Rare | — | 1 | |
| Hyperthyroidism, non-autoimmune (HTNA) | N/A | — | 1 | |
| Hyperthyroxinemia, dystransthyretinemic (DTTRH) | Ultra-Rare | — | 1 | |
| Hypertriglyceridemia, transient infantile (HTGTI) | Ultra-Rare | — | 1 | |
| Hypogonadotropic hypogonadism 24 with or without anosmia (HH24) | N/A | — | 1 | |
| Hypoinsulinemic hypoglycemia with hemihypertrophy (HIHGHH) | Ultra-Rare | — | 1 | |
| Hypothyroidism, congenital, non-goitrous, 1 (CHNG1) | N/A | — | 1 | |
| Ichthyosis-sclerosing cholangitis neonatal syndrome (NISCH) | Ultra-Rare | — | 1 | |
| Immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) | Ultra-Rare | — | 1 | |
| Pancreatitis, hereditary (PCTT) | Very Rare | — | 1 | |
| Pituitary hormone deficiency, combined or isolated, 8 (CPHD8) | N/A | — | 1 | |
| Premature ovarian failure 21 (POF21) | N/A | — | 1 | |
| Primary pigmented nodular adrenocortical disease 1 (PPNAD1) | Ultra-Rare | — | 1 | |
| Primary pigmented nodular adrenocortical disease 4 (PPNAD4) | Ultra-Rare | — | 1 |