Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9820
Gene Symbol: CUL7
CUL7
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 GeneticVariation CLINVAR Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. 30980518

2019
Entrez Id: 89953
Gene Symbol: KLC4
KLC4
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 GeneticVariation CLINVAR Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. 30980518

2019
Entrez Id: 23363
Gene Symbol: OBSL1
OBSL1
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 GeneticVariation CLINVAR Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. 30980518

2019
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980

2015
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 CausalMutation CLINVAR

Entrez Id: 27245
Gene Symbol: AHDC1
AHDC1
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 CausalMutation CLINVAR

Entrez Id: 55023
Gene Symbol: PHIP
PHIP
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 GeneticVariation CLINVAR

Entrez Id: 6884
Gene Symbol: TAF13
TAF13
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 CausalMutation CLINVAR

Entrez Id: 10847
Gene Symbol: SRCAP
SRCAP
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 CausalMutation CLINVAR

Entrez Id: 79631
Gene Symbol: EFL1
EFL1
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 GeneticVariation CLINVAR