syndromic intellectual disability (Q18553536)
intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms
Language:
Current Data About syndromic intellectual disability
(P31) (Q929833)

(Q112193867)

(P279) (Q183560)
(P248)
(P813) Saturday, July 28, 2018
(P5270) MONDO_0015162

(P373) Syndromes with intellectual disability

(P910) (Q30822641)

(P2293) (Q18031610)
(P248)

(Q18032252)
(P248)

(Q18030282)
(P248)

(Q17835924)
(P248)
(P813) Monday, August 31, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/1d586d93-7066-4db0-b623-8b7e3eafdc06--2020-08-20T03:25:48

(Q18037904)
(P248)
(P813) Monday, September 7, 2020
(P854) https://search.clinicalgenome.org/kb/gene-validity/582999f6-b3b4-46de-90a0-8f44e22df469--2020-09-01T16:00:00

(Q18037142)
(P248)
(P813) Monday, December 27, 2021
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_41758f8d-1f99-47fa-beb6-c327fa6cb940-2021-04-21T040000.000Z

(Q18036678)
(P248)
(P813) Tuesday, January 25, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_32897f25-e36a-4ec8-9401-0374a95e06a5-2020-08-18T160000.000Z

(Q18033279)
(P248)
(P813) Monday, January 31, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_7f64ee7f-13a7-4a2d-b1a2-ad6c9e63cab3-2021-06-16T180000.000Z

(Q18043138)
(P248)
(P813) Monday, March 14, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_79c712d0-ac0e-4bf0-8e68-bd598b3bca42-2021-08-04T160000.000Z

(Q21163346)
(P248)
(P813) Monday, March 28, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_f1cbcd7b-83e2-47c1-b708-c9052502e639-2021-07-21T160000.000Z

(Q18041700)
(P248)
(P813) Monday, April 4, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_cedd313e-b43b-4212-840b-7d4172258b16-2021-09-28T115443.696Z

(Q18027119)
(P248)
(P813) Monday, May 23, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_1e0e605f-c82a-4e34-b913-8dc6b72b4881-2019-06-19T160000.000Z

(Q4864556)
(P248)
(P813) Monday, May 23, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_ff3b6c9b-4c51-4414-b92c-20e45758ab61-2021-11-18T192046.961Z

(Q18032355)
(P248)
(P813) Monday, December 27, 2021
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_de3c113b-0a7d-454d-88e3-faf4f1fdb9ac-2021-06-02T160000.000Z

(Q18033160)
(P248)
(P813) Monday, January 3, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_c594bcfa-2b2c-425a-8285-74bae8e01da8-2021-12-31T225720.705Z

(Q18036517)
(P248)
(P813) Monday, January 3, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_661c140f-11a3-46f8-b001-14a2314582e4-2021-12-15T170000.000Z

(Q18032697)
(P248)
(P813) Monday, January 17, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_86ec74ba-6b12-42ea-bc06-58af4fd6b7a4-2021-10-05T160000.000Z

(Q18030728)
(P248)
(P813) Monday, January 17, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_4b43ff91-1ea4-475b-97d9-6fbda924ea16-2022-01-12T055053.721Z

(Q18036827)
(P248)
(P813) Friday, February 25, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_37e4fa5a-05b7-4cee-b43a-eb58488346bd-2022-01-19T170000.000Z

(Q18032981)
(P248)
(P813) Thursday, May 19, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_a93ec2cb-1632-4439-bdd9-4bcae1bb779f-2022-02-15T170000.000Z

(Q18036648)
(P248)
(P813) Thursday, May 19, 2022
(P854) https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_a9300a41-dcac-4842-855d-01804e18d599-2022-01-19T170000.000Z

(P2888) http://purl.obolibrary.org/obo/DOID_0050888
(P248)
(P813) Monday, November 30, 2020
(P699) DOID:0050888

http://identifiers.org/doid/DOID:0050888
(P248)
(P854) https://registry.identifiers.org/registry/doid

http://www.orpha.net/ORDO/Orphanet_102369

(P5008) (Q4099686)

other details
aliases rare syndromic intellectual disability
description intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms

External Links
(P699) DOID:0050888
(P1550) 102369
(P2892) C5681780
(P5270) MONDO_0015162