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GlyCosmos Diseases

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

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6026 - 6050** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:6225	Cronkhite-Canada syndrome Aliases: gastric Cronkhite Canada polyposis polyposis, skin pigmentation, alopecia, and fingernail changes	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:6084	childhood ovarian germ cell tumor Aliases: paediatric Ovarian germ cell neoplasm paediatric ovarian germ cell tumour pediatric Ovarian germ cell neoplasm pediatric ovarian germ cell tumor	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:3001	female reproductive endometrioid cancer Aliases: endometrioid neoplasm endometrioid tumor	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:5830	cervical endometrioid adenocarcinoma Aliases: endometrioid carcinoma of the Cervix Uteri	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:4586	familial meningioma	PTEN	5728	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:4205	cerebellum cancer Aliases: cerebellar cancer malignant tumor of Cerebellum	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:7763	carcinoma of supraglottis Aliases: Supraglottic carcinoma	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:264	hemangiopericytoma Aliases: Haemangiopericytic meningioma hemangiopericytoma, malignant malignant hemangiopericytoma	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:5890	malignant adult ependymoma	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:0060488	Pitt-Hopkins syndrome	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:0060867	macrocephaly-autism syndrome Aliases: macrocephaly-intellectual disability-autism syndrome	PTEN	5728	Homo sapiens (human)	DisGeNET Alliance of Genome Resources
DOID:7689	leptomeninges sarcoma Aliases: Leptomeningeal sarcoma sarcoma of Leptomeninges	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:3742	bladder squamous cell carcinoma Aliases: Epidermoid carcinoma of the urinary bladder squamous cell carcinoma of bladder	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:5172	endometrium carcinoma in situ Aliases: carcinoma in situ of endometrium endometrial carcinoma in situ	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:6496	obsolete extraskeletal myxoid chondrosarcoma	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:8368	chordoid meningioma Aliases: meningioma, chordoid	PTEN	5728	Homo sapiens (human)	DisGeNET DisGeNET
DOID:10071	larynx squamous papilloma Aliases: Laryngeal Squamous Cell Papilloma	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:3279	spindle cell thymoma Aliases: Medullary Thymoma Thymoma, medullary	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:3875	thrombophlebitis Aliases: Phlebitis and thrombophlebitis of superficial vessels of lower extremities Superficial thrombophlebitis of leg Thrombophlebitis of a superficial leg vein Thrombophlebitis of superficial veins of lower extremity	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:2938	Epstein-Barr virus infectious disease Aliases: EBV Infection Epstein-Barr virus infection	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080072	intestinal pseudo-obstruction Aliases: Chronic intestinal pseudo-obstruction neuronal intestinal dysplasia	PTEN	5728	Homo sapiens (human)	Alliance of Genome Resources
DOID:2495	senile angioma Aliases: Senile hemangioma Senile naevus of skin	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:7587	supraglottis squamous cell carcinoma Aliases: Epidermoid carcinoma of the Supraglottis	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:12211	filarial elephantiasis Aliases: Bancroftian elephantiasis Bancroftian filarial chyluria Lymphatic filariasis elephantiasis of eyelid	PTEN	5728	Homo sapiens (human)	DisGeNET
DOID:13042	persistent fetal circulation syndrome Aliases: Fetal circulation Persistent fetal circulation Persistent foetal circulation congenital alveolar capillary dysplasia with misalignment of pulmonary veins persistent foetal circulation syndrome persistent pulmonary hypertension of the newborn	PTEN	5728	Homo sapiens (human)	DisGeNET Alliance of Genome Resources

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