DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C1621958 | Glioblastoma Multiforme | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0019269 | Hermaphroditism | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0007847 | Malignant tumor of cervix | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C2973529 | Leukocytoclastic vasculitis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0023343 | Leprosy | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0001144 | Acne Vulgaris | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0205645 | Adenocarcinoma, Tubular | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0751529 | Stuttering, Developmental | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0032002 | Pituitary Diseases | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1704273 | Endometrial Polyp | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0023601 | Leydig Cell Tumor | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0038220 | Status Epilepticus | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0038454 | Cerebrovascular accident | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0011265 | Presenile dementia | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0476254 | Dyslexia | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C4048328 | cervical cancer | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0442874 | Neuropathy | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0524620 | Metabolic Syndrome X | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0206630 | Endometrial Stromal Sarcoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0032051 | Placental Insufficiency | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0017411 | Female Genital Diseases | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0001618 | Tumors of Adrenal Cortex | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0025202 | melanoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0156369 | Uterine Polyp | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0242350 | Erectile dysfunction | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024