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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6826 - 6850** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:3620	central nervous system cancer Aliases: CNS neoplasm central nervous system tumor central nervous system tumors malignant neoplasm of central nervous system malignant tumor of CNS neoplasm of central nervous system	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:1319	brain cancer Aliases: BT - Brain tumour adult brain tumor adult malignant brain neoplasm brain neoplasm brain neoplasm, adult malignant brain tumour malignant primary brain neoplasm malignant primary brain tumor malignant tumor of Brain malignant tumor of adult brain neoplasm of brain primary brain neoplasm primary brain tumor primary malignant neoplasm of brain tumor of the Brain	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:2736	Hajdu-Cheney syndrome Aliases: Cheney syndrome HJCYS SFPKS acroosteolysis with osteoporosis and changes in skull and mandible arthrodentoosteodysplasia serpentine fibula-polycystic kidney syndrome	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:299	adenocarcinoma	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080333	aortic valve disease 1	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111343	lateral meningocele syndrome Aliases: Lehman syndrome	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050523	adult T-cell leukemia/lymphoma Aliases: Adult T-cell leukemia/lymphoma (HTLV-1 positive) adult T-cell leukemia	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080109	infantile myofibromatosis Aliases: lipofibromatosis	N tor	31293 35717	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9245	Alagille syndrome Aliases: Alagille-Watson syndrome Arteriohepatic dysplasia	N Ser	31293 43275	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070069	autosomal dominant intellectual developmental disorder 39 Aliases: MRD39 autosomal dominant mental retardation 39 autosomal dominant non-syndromic intellectual disability 39	Myt1l	17933	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110445	dilated cardiomyopathy 1KK Aliases: CMD1KK	Mypn	68802	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110933	nemaline myopathy 11 Aliases: NEM11 nemaline myopathy 11, autosomal recessive	Mypn	68802	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110322	hypertrophic cardiomyopathy 16 Aliases: CMH16 cardiomyopathy familial hypertrophic 16	Myoz2	59006	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1068	juvenile glaucoma Aliases: Glaucoma of childhood	Myoc	81523	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1068	juvenile glaucoma Aliases: Glaucoma of childhood	Myoc	17926	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14159	obstructive hydrocephalus	Myo9a	270163	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110495	autosomal recessive nonsyndromic deafness 37 Aliases: DFNB37 autosomal recessive deafness 37	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110552	autosomal dominant nonsyndromic deafness 22 Aliases: DFNA22 autosomal dominant deafness 22	Myo6	17920	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060832	Griscelli syndrome type 1 Aliases: GS1 Griscelli syndrome with neurological impairment Griscelli syndrome, cutaneous and neurological type Griscelli-Prunieras syndrome type 1 hypopigmentation-neurologic impairment syndrome	Myo5a	25017	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060832	Griscelli syndrome type 1 Aliases: GS1 Griscelli syndrome with neurological impairment Griscelli syndrome, cutaneous and neurological type Griscelli-Prunieras syndrome type 1 hypopigmentation-neurologic impairment syndrome	Myo5a	17918	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080592	Klippel-Feil syndrome 4	Myo18b	74376	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110314	hypertrophic cardiomyopathy 8 Aliases: cardiomyopathy hypertrophic mid-left ventricular chamber type 1 cardiomyopathy, familial hypertrophic, 8	Myl3	24585	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110314	hypertrophic cardiomyopathy 8 Aliases: cardiomyopathy hypertrophic mid-left ventricular chamber type 1 cardiomyopathy, familial hypertrophic, 8	Myl3	17897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110316	hypertrophic cardiomyopathy 10 Aliases: CMH10 cardiomyopathy, familial hypertrophic, 10	Myl2	363925	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081346	congenital myopathy 14	Myl1	17901	Mus musculus (house mouse)	Alliance of Genome Resources

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