Syndromic X-Linked Intellectual Disability
Disease ID: disease_node_13590
Connections displayed (default: 10).
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| Dbxref | MIM:PS309510 |
|---|---|
| Subclassof | DOID_0050888, DOID_0050735 |
| Data Source | DOID |
| Synonyms | syndromic X-linked mental retardation |
| Doid Label | syndromic X-linked intellectual disability |
| Doid Description | A syndromic intellectual disability characterized by an X-linked inheritance pattern. NT MGI. |
| Has Material Basis In | GENO_0000936 |
| Disease Node Id | disease_node_13590 |
| Doid Id | DOID_0060309 |
| Label | Syndromic X-Linked Intellectual Disability |
- Incoming r'ship
SUBCLASS_OFto/from X-Linked Mental Retardation With Cerebellar Hypoplasia And Distinctive Facial Appearance(ID:disease_node_13601) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Intellectual Developmental Disorder 109(ID:disease_node_13599) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Intellectual Disability-Cardiomegaly-Congestive Heart Failure Syndrome(ID:disease_node_19235) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Mental Retardation Gustavson Type(ID:disease_node_13597) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Mental Retardation-Hypotonic Facies Syndrome-1(ID:disease_node_13600) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Intellectual Developmental Disorder 108(ID:disease_node_19232) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Intellectual Disability-Short Stature-Overweight Syndrome(ID:disease_node_13594) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome(ID:disease_node_19236) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Najm Type(ID:disease_node_13615) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Cabezas Type(ID:disease_node_19240) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Chudley-Schwartz Type(ID:disease_node_13606) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Tonne-Kalscheuer Syndrome(ID:disease_node_13595) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability 17(ID:disease_node_13619) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Pilorge Type(ID:disease_node_13605) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Mental Retardation 35(ID:disease_node_13603) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Shashi Type(ID:disease_node_19237) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Nascimento Type(ID:disease_node_19241) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Mental Retardation Hough Type(ID:disease_node_13602) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Shrimpton Type(ID:disease_node_13611) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Raymond Type(ID:disease_node_19238) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Type 10(ID:disease_node_13613) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Hedera Type(ID:disease_node_13616) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndromic Intellectual Disability(ID:disease_node_16360) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Wilson-Turner Syndrome(ID:disease_node_13610) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability 34(ID:disease_node_13607) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Turner Type(ID:disease_node_13612) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Stocco Dos Santos Type X-Linked Intellectual Disability(ID:disease_node_13591) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability 12(ID:disease_node_13618) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability 94(ID:disease_node_19239) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Monogenic Disease(ID:disease_node_13360) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Van Esch-O'Driscoll Syndrome(ID:disease_node_13592) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Developmental Disorder Bain Type(ID:disease_node_13604) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Wieacker-Wolff Syndrome(ID:disease_node_13609) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disorder Lujan-Fryns-Type(ID:disease_node_13598) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Claes-Jensen Type(ID:disease_node_13614) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Syndromic X-Linked Intellectual Disability Snyder Type(ID:disease_node_13620) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Renpenning Syndrome(ID:disease_node_19229) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Raynaud-Claes Syndrome(ID:disease_node_13589) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Paganini-Miozzo Syndrome(ID:disease_node_19233) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Prieto Syndrome(ID:disease_node_13617) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mullegama-Klein-Martinez Syndrome(ID:disease_node_19231) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Female-Restricted Wieacker-Wolff Syndrome(ID:disease_node_19242) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Female-Restricted Syndromic X-Linked Intellectual Disability 99(ID:disease_node_13596) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Corpus Callosum Agenesis-Intellectual Disability-Coloboma-Micrognathia Syndrome(ID:disease_node_13608) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Deafness-Intellectual Disability, Martin-Probst Type Syndrome(ID:disease_node_19234) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Basilicata-Akhtar Syndrome(ID:disease_node_13593) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Armfield Syndrome(ID:disease_node_19230) (Disease)