DisGeNET

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
Displaying entries 44626 - 44650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C3489396 Hypogonadism, Isolated Hypogonadotropic CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C1568363 Tendinosis CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0020635 Hypopituitarism CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0027832 Neurofibromatosis 2 CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0221392 Atrophic Vaginitis CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0158447 Idiopathic osteoporosis CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0018799 Heart Diseases CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0027086 Myoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0205644 Carcinoma, Granular Cell CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0002453 Amenorrhea CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0007112 Adenocarcinoma of prostate CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C3489532 Cone-Rod Dystrophy 2 CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0153633 Malignant neoplasm of brain CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C1510586 Autism Spectrum Disorders CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0003811 Cardiac Arrhythmia CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0546837 Malignant neoplasm of esophagus CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0220668 Congenital contractural arachnodactyly CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0236663 Alcohol withdrawal syndrome CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0342386 Follicle stimulating hormone deficiency CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0936016 Testicular Feminization CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0004352 Autistic Disorder CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0345904 Malignant neoplasm of liver CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0151436 Vasculitis, Leukocytoclastic, Cutaneous CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0008354 Cholera CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511
C0855173 Placental Choriocarcinoma CYP19A1 1588 cytochrome P450 family 19 subfamily A member 1 P11511

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024