25 Jan 2021
Intellectual disability - microarray and sequencing v3.734
FGFR1
Arina Puzriakova Phenotypes for gene: FGFR1 were changed from Hartsfield syndrome, OMIM:615465; Pfeiffer syndrome, OMIM:101600 to Hartsfield syndrome, OMIM:615465; Pfeiffer syndrome, OMIM:101600; Encephalocraniocutaneous lipomatosis, somatic mosaic, OMIM:613001
25 Jan 2021
Intellectual disability - microarray and sequencing v3.733
FGFR1
Arina Puzriakova Publications for gene: FGFR1 were set to 28825856
25 Jan 2021
Intellectual disability - microarray and sequencing v3.732
FGFR1
Arina Puzriakova Phenotypes for gene: FGFR1 were changed from Encephalocraniocutaneous lipomatosis, 613001; KALLMANN SYNDROME TYPE 2; Pfeiffer syndrome,101600 to Hartsfield syndrome, OMIM:615465; Pfeiffer syndrome, OMIM:101600
25 Jan 2021
Intellectual disability - microarray and sequencing v3.731
FGFR1
Arina Puzriakova reviewed gene: FGFR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
03 Feb 2020
Intellectual disability - microarray and sequencing v3.0
FGFR1
Zornitza Stark edited their review of gene: FGFR1: Added comment: Gene causes several phenotypes but this specific phenotype caused by germline variants is associated with significant ID.; Changed publications: 23812909; Changed phenotypes: Hartsfield syndrome, MIM# 615465
28 Sep 2018
Intellectual disability - microarray and sequencing v2.468
FGFR1
Louise Daugherty Source Victorian Clinical Genetics Services was added to FGFR1.
12 Sep 2018
Intellectual disability - microarray and sequencing v2.408
FGFR1
Louise Daugherty reviewed gene: FGFR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
17 Jun 2018
Intellectual disability - microarray and sequencing
FGFR1
Zornitza Stark reviewed gene: FGFR1
02 Aug 2017
Intellectual disability - microarray and sequencing
FGFR1
BRIDGE consortium edited their review of FGFR1
27 Jul 2017
Intellectual disability - microarray and sequencing
FGFR1
BRIDGE consortium edited their review of FGFR1
19 Jul 2017
Intellectual disability - microarray and sequencing
FGFR1
BRIDGE consortium reviewed FGFR1