X-Linked Domit Disease

Disease ID: disease_node_13587

Connections displayed (default: 10).

Plants :

Formulations :

Phytochemicals :

Other Diseases :

Loading graph...

ℹ️ Click here to know more about the properties

Subclassof	DOID_0050735
Data Source	DOID
Doid Label	X-linked domit disease
Doid Description	A X-linked monogenic disease that has_material_basis_in domit inheritance.
Disease Node Id	disease_node_13587
Doid Id	DOID_0080009
Label	X-Linked Domit Disease

Incoming r'ship SUBCLASS_OF to/from X-Linked Alport Syndrome(ID:disease_node_19098) (Disease)
Outgoing r'ship SUBCLASS_OF to/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease)
Incoming r'ship SUBCLASS_OF to/from X-Linked Chondrodysplasia Punctata 2(ID:disease_node_19139) (Disease)
Incoming r'ship SUBCLASS_OF to/from Reducing Body Myopathy 1A(ID:disease_node_18985) (Disease)
Incoming r'ship SUBCLASS_OF to/from Raynaud-Claes Syndrome(ID:disease_node_13589) (Disease)
Incoming r'ship SUBCLASS_OF to/from Primary Ovarian Insufficiency 2A(ID:disease_node_17220) (Disease)
Incoming r'ship SUBCLASS_OF to/from Neurodegeneration With Brain Iron Accumulation 5(ID:disease_node_16092) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 1(ID:disease_node_16336) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 41(ID:disease_node_16318) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 98(ID:disease_node_16331) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 63(ID:disease_node_16325) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 19(ID:disease_node_16354) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 2(ID:disease_node_16357) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 89(ID:disease_node_16343) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 107(ID:disease_node_16321) (Disease)
Incoming r'ship SUBCLASS_OF to/from Non-Syndromic X-Linked Intellectual Disability 91(ID:disease_node_16332) (Disease)
Incoming r'ship SUBCLASS_OF to/from Linear Skin Defects With Multiple Congenital Anomalies 3(ID:disease_node_19245) (Disease)
Incoming r'ship SUBCLASS_OF to/from Linear Skin Defects With Multiple Congenital Anomalies 2(ID:disease_node_19244) (Disease)
Incoming r'ship SUBCLASS_OF to/from Holoprosencephaly 13, X-Linked(ID:disease_node_13586) (Disease)
Incoming r'ship SUBCLASS_OF to/from Familial Hypophosphatemic Rickets(ID:disease_node_11643) (Disease)
Incoming r'ship SUBCLASS_OF to/from Female-Restricted Syndromic X-Linked Intellectual Disability 99(ID:disease_node_13596) (Disease)
Incoming r'ship SUBCLASS_OF to/from Fragile X Syndrome(ID:disease_node_3317) (Disease)
Incoming r'ship SUBCLASS_OF to/from Focal Dermal Hypoplasia(ID:disease_node_3276) (Disease)
Incoming r'ship SUBCLASS_OF to/from Female-Restricted Wieacker-Wolff Syndrome(ID:disease_node_19242) (Disease)
Incoming r'ship SUBCLASS_OF to/from Glycogen Storage Disease Type Iib(ID:disease_node_11501) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 36(ID:disease_node_16196) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 9(ID:disease_node_16273) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Nystagmus 5(ID:disease_node_19246) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 2(ID:disease_node_19095) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 85(ID:disease_node_16258) (Disease)
Incoming r'ship SUBCLASS_OF to/from Deafness, Dystonia, And Cerebral Hypomyelination(ID:disease_node_13588) (Disease)
Incoming r'ship SUBCLASS_OF to/from Cornelia De Lange Syndrome 5(ID:disease_node_19092) (Disease)
Incoming r'ship SUBCLASS_OF to/from Developmental And Epileptic Encephalopathy 2(ID:disease_node_16198) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease X-Linked Domit 1(ID:disease_node_18825) (Disease)
Incoming r'ship SUBCLASS_OF to/from Charcot-Marie-Tooth Disease X-Linked Domit 6(ID:disease_node_18826) (Disease)
Incoming r'ship SUBCLASS_OF to/from Coffin-Lowry Syndrome(ID:disease_node_11156) (Disease)
Incoming r'ship SUBCLASS_OF to/from Congenital Disorder Of Glycosylation Type Iim(ID:disease_node_19247) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xx Sex Reversal 3(ID:disease_node_17162) (Disease)
Incoming r'ship SUBCLASS_OF to/from Alpha Thalassemia-X-Linked Intellectual Disability Syndrome(ID:disease_node_17084) (Disease)
Incoming r'ship SUBCLASS_OF to/from Amelogenesis Imperfecta Type 1E(ID:disease_node_18103) (Disease)
Incoming r'ship SUBCLASS_OF to/from 46,Xx Sex Reversal 1(ID:disease_node_17163) (Disease)

Back to Browse Back to Home

GRAYU Website

Grayu

X-Linked Domit Disease

Graph

Disease Properties

Associated Connections 41

Disease Connections 41