Monogenic Disease

Disease ID: disease_node_13650

Connections displayed (default: 10).

Plants :

Formulations :

Phytochemicals :

Other Diseases :

Loading graph...

ℹ️ Click here to know more about the properties

Subclassof	DOID_630
Data Source	DOID
Doid Label	monogenic disease
Doid Description	A genetic disease that is the result of one or more abnormal alleles and may be domit, semi-domit, or recessive.
Disease Node Id	disease_node_13650
Doid Id	DOID_0050177
Label	Monogenic Disease

Incoming r'ship SUBCLASS_OF to/from Schizophrenia 9(ID:disease_node_15934) (Disease)
Incoming r'ship SUBCLASS_OF to/from Y-Linked Monogenic Disease(ID:disease_node_14949) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease)
Incoming r'ship SUBCLASS_OF to/from Shox-Related Short Stature(ID:disease_node_15699) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 14(ID:disease_node_15929) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 16(ID:disease_node_15927) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 13(ID:disease_node_15930) (Disease)
Incoming r'ship SUBCLASS_OF to/from Schizophrenia 18(ID:disease_node_15926) (Disease)
Incoming r'ship SUBCLASS_OF to/from Anterior Segment Dysgenesis(ID:disease_node_19120) (Disease)
Incoming r'ship SUBCLASS_OF to/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease)
Incoming r'ship SUBCLASS_OF to/from Camurati-Engelmann Syndrome(ID:disease_node_2502) (Disease)
Incoming r'ship SUBCLASS_OF to/from Bartter Syndrome(ID:disease_node_1490) (Disease)
Incoming r'ship SUBCLASS_OF to/from Brugada Syndrome(ID:disease_node_11785) (Disease)
Incoming r'ship SUBCLASS_OF to/from Chondrodysplasia Punctata(ID:disease_node_2065) (Disease)
Incoming r'ship SUBCLASS_OF to/from Catecholaminergic Polymorphic Ventricular Tachycardia(ID:disease_node_19145) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract(ID:disease_node_1890;disease_node_13651) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cone-Rod Dystrophy(ID:disease_node_16580) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ciliopathy(ID:disease_node_14682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1J(ID:disease_node_16902) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1I(ID:disease_node_16911) (Disease)
Incoming r'ship SUBCLASS_OF to/from De Lange Syndrome(ID:disease_node_2376) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1K(ID:disease_node_16905) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1W(ID:disease_node_16896) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1L(ID:disease_node_16906) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Bb(ID:disease_node_16884) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Ff(ID:disease_node_16883) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1H(ID:disease_node_16913) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Q(ID:disease_node_16900) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Ee(ID:disease_node_16889) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Gg(ID:disease_node_16907) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1O(ID:disease_node_16891) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1Z(ID:disease_node_16908) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1G(ID:disease_node_16912) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1M(ID:disease_node_16893) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1T(ID:disease_node_16890) (Disease)
Incoming r'ship SUBCLASS_OF to/from Dilated Cardiomyopathy 1P(ID:disease_node_16903) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group G(ID:disease_node_15298) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hemophagocytic Lymphohistiocytosis 5(ID:disease_node_18243) (Disease)
Incoming r'ship SUBCLASS_OF to/from Gene Duplication Disease(ID:disease_node_19116) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group J(ID:disease_node_15287) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group N(ID:disease_node_15290) (Disease)
Incoming r'ship SUBCLASS_OF to/from Erythrokeratodermia Variabilis(ID:disease_node_12187) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fanconi Anemia Complementation Group F(ID:disease_node_15296) (Disease)
Incoming r'ship SUBCLASS_OF to/from Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors(ID:disease_node_17044) (Disease)
Incoming r'ship SUBCLASS_OF to/from Isolated Microphthalmia 4(ID:disease_node_16611) (Disease)
Incoming r'ship SUBCLASS_OF to/from Inflammatory Bowel Disease 1(ID:disease_node_14190) (Disease)
Incoming r'ship SUBCLASS_OF to/from Infantile Histiocytoid Cardiomyopathy(ID:disease_node_16949) (Disease)
Incoming r'ship SUBCLASS_OF to/from Leber Congenital Amaurosis 7(ID:disease_node_19106) (Disease)
Incoming r'ship SUBCLASS_OF to/from Lambda 5 Deficiency(ID:disease_node_17348) (Disease)
Incoming r'ship SUBCLASS_OF to/from Multiple Epiphyseal Dysplasia Due To Collagen 9 Anomaly(ID:disease_node_15636) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 14(ID:disease_node_15625) (Disease)
Incoming r'ship SUBCLASS_OF to/from Noonan Syndrome(ID:disease_node_5622) (Disease)
Incoming r'ship SUBCLASS_OF to/from Nephritis, Hereditary(ID:disease_node_5489) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteogenesis Imperfecta Type 6(ID:disease_node_15618) (Disease)
Incoming r'ship SUBCLASS_OF to/from Posterior Polymorphous Corneal Dystrophy 3(ID:disease_node_17144) (Disease)
Incoming r'ship SUBCLASS_OF to/from Postural Orthostatic Tachycardia Syndrome(ID:disease_node_11999) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Congenital Glaucoma(ID:disease_node_14333) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Genetic Diseases, Inborn(ID:disease_node_11057) (Disease)

Back to Browse Back to Home

GRAYU Website

Grayu

Monogenic Disease

Graph

Disease Properties

Associated Connections 58

Disease Connections 58