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 16776 - 16800 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0015469 Facial paralysis ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0023794 Lipoidosis ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0346647 Malignant neoplasm of pancreas ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0025007 Measles ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0017185 Gastrointestinal Neoplasms ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0205696 Anaplastic carcinoma ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0019348 Herpes Simplex Infections ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C1864100 PSEUDOHYPOPARATHYROIDISM, TYPE IB ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0085084 Motor Neuron Disease ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C1851584 Childhood Ependymoma ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0023521 Globoid cell leukodystrophy ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0037822 Speech Disorders ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0032285 Pneumonia ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0158981 Neonatal diabetes mellitus ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0004903 Beckwith-Wiedemann Syndrome ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C1458155 Mammary Neoplasms ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0558356 Malignant melanoma of eye ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0014474 Ependymoma ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0029456 Osteoporosis ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0007113 Rectal Carcinoma ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0699790 Colon Carcinoma ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0020456 Hyperglycemia ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0002395 Alzheimer's Disease ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0041408 Turner Syndrome ASAH1 427 N-acylsphingosine amidohydrolase 1 Q13510
C0013274 Patent ductus arteriosus ART3 419 ADP-ribosyltransferase 3 Q13508

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Last updated: August 19, 2024