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 |
---|---|---|---|---|---|
C0870082 | Hyperkeratosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0037772 | Spastic Paraplegia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0035334 | Retinitis Pigmentosa | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0027092 | Myopia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0342482 | X-linked Adrenal Hypoplasia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0020758 | Congenital ichthyosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0029422 | Osteochondrodysplasias | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C3714756 | Intellectual Disability | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0085636 | Photophobia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0042109 | Urticaria | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0242383 | Age related macular degeneration | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0007131 | Non-Small Cell Lung Carcinoma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0011644 | Scleroderma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0687120 | Nephronophthisis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0022578 | Keratoconus | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0027765 | nervous system disorder | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0020258 | Hydrocephalus, Normal Pressure | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0011351 | Dental Enamel Hypoplasia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0036439 | Scoliosis, unspecified | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0079583 | Ichthyosiform Erythroderma, Congenital | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0036572 | Seizures | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0025958 | Microcephaly | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0041834 | Erythema | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0034372 | Quadriplegia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
C0013336 | Dwarfism | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
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