Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 Biomarker GENOMICS_ENGLAND Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway. 27363716

2016

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 Biomarker GENOMICS_ENGLAND FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies. 25759380

2015

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 Biomarker GENOMICS_ENGLAND Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations. 25394172

2015

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 GeneticVariation UNIPROT In this report, we describe two siblings with Hartsfield syndrome and a novel de novo FGFR1 mutation suggesting gonadal mosaicism. 24888332

2014

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 GeneticVariation UNIPROT Dominant or recessive FGFR1 mutations are responsible for Hartsfield syndrome, consistent with the known roles of FGFR1 in vertebrate ontogeny and conditional Fgfr1-deficient mice. 23812909

2013

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 GermlineCausalMutation ORPHANET Dominant or recessive FGFR1 mutations are responsible for Hartsfield syndrome, consistent with the known roles of FGFR1 in vertebrate ontogeny and conditional Fgfr1-deficient mice. 23812909

2013

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 Biomarker GENOMICS_ENGLAND Dominant or recessive FGFR1 mutations are responsible for Hartsfield syndrome, consistent with the known roles of FGFR1 in vertebrate ontogeny and conditional Fgfr1-deficient mice. 23812909

2013

Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
0.750 Biomarker GENOMICS_ENGLAND Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. 12627230

2003