X-Linked Monogenic Disease

Disease ID: disease_node_13360

Connections displayed (default: 10).

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Subclassof	DOID_0050177
Data Source	DOID
Doid Label	X-linked monogenic disease
Doid Description	A monogenic disease that has_material_basis_in mutations in genes on the X chromosome.
Disease Node Id	disease_node_13360
Doid Id	DOID_0050735
Label	X-Linked Monogenic Disease

Incoming r'ship SUBCLASS_OF to/from X-Linked Hereditary Ataxia(ID:disease_node_16058) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Domit Disease(ID:disease_node_13587) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Lissencephaly 1(ID:disease_node_19264) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Central Diabetes Insipidus(ID:disease_node_19683) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 4(ID:disease_node_15187) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 6(ID:disease_node_15185) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Hypoparathyroidism(ID:disease_node_17237) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Retinitis Pigmentosa And Sinorespiratory Infections(ID:disease_node_13361) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 5(ID:disease_node_15186) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Panhypopituitarism(ID:disease_node_13359) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Lissencephaly 2(ID:disease_node_19265) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Cleft Palate With Or Without Ankyloglossia(ID:disease_node_14025) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Monogenic Disease(ID:disease_node_13650) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Nonsyndromic Deafness(ID:disease_node_14955) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Exudative Vitreoretinopathy 2(ID:disease_node_17038) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Spermatogenic Failure 8(ID:disease_node_15183) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic Microphthalmia 13(ID:disease_node_16599) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic X-Linked Intellectual Disability(ID:disease_node_13590) (Disease)
Incoming r'ship SUBCLASS_OF to/from Syndromic Microphthalmia 1(ID:disease_node_16603) (Disease)
Incoming r'ship SUBCLASS_OF to/from Reducing Body Myopathy 1B(ID:disease_node_18972) (Disease)
Incoming r'ship SUBCLASS_OF to/from Retinitis Pigmentosa 24(ID:disease_node_15830) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 1(ID:disease_node_17221) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 4(ID:disease_node_17217) (Disease)
Incoming r'ship SUBCLASS_OF to/from Ogden Syndrome(ID:disease_node_19687) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability(ID:disease_node_16316) (Disease)
Incoming r'ship SUBCLASS_OF to/from Osteochondrodysplasias(ID:disease_node_5766) (Disease)
Incoming r'ship SUBCLASS_OF to/from Meester-Loeys Syndrome(ID:disease_node_19688) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fetal Akinesia Deformation Sequence Syndrome X-Linked(ID:disease_node_19105) (Disease)
Incoming r'ship SUBCLASS_OF to/from Corpus Callosum Agenesis-Abnormal Genitalia Syndrome(ID:disease_node_19682) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nonspherocytic Hemolytic Anemia 1(ID:disease_node_15268) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 90(ID:disease_node_16257) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Bilateral Absence Of Vas Deferens(ID:disease_node_17151) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cataract 40(ID:disease_node_13661) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xy Sex Reversal 2(ID:disease_node_17154) (Disease)

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X-Linked Monogenic Disease

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Disease Properties

Associated Connections 35

Disease Connections 35