FGF8, fibroblast growth factor 8, 2253

N. diseases: 212; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3552574
Disease: HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA 		0.600 CausalMutation disease CLINVAR
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.560 Biomarker disease CTD_human
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		0.500 Biomarker disease MGD
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.450 GeneticVariation disease CLINVAR
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.450 Biomarker disease HPO
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.450 CausalMutation disease CLINVAR
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.400 Biomarker disease HPO
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.400 Biomarker disease HPO
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		0.400 GermlineCausalMutation disease ORPHANET
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		0.400 GeneticVariation disease CLINVAR
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.300 Biomarker disease HPO
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.300 Biomarker disease MGD
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		0.300 GermlineCausalMutation disease ORPHANET
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		0.300 GermlineCausalMutation disease ORPHANET
CUI: C1563719
Disease: Kallmann Syndrome 1
Kallmann Syndrome 1 		0.300 Biomarker disease CTD_human
CUI: C1563720
Disease: Kallmann Syndrome 2 (disorder)
Kallmann Syndrome 2 (disorder) 		0.300 Biomarker disease CTD_human
CUI: C2930927
Disease: Kallmann syndrome, type 3, recessive
Kallmann syndrome, type 3, recessive 		0.300 Biomarker disease CTD_human
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.160 Biomarker disease HPO
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		0.110 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.110 Biomarker disease HPO
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		0.110 Biomarker disease HPO
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		0.110 Biomarker disease HPO
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		0.110 Biomarker phenotype HPO
CUI: C0003126
Disease: Anosmia
Anosmia 		0.100 Biomarker phenotype HPO
CUI: C0003467
Disease: Anxiety
Anxiety 		0.100 Biomarker disease HPO