FEZF1, FEZ family zinc finger 1, 389549

N. diseases: 73; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty 		0.100 Biomarker phenotype HPO
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker phenotype HPO
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		0.100 Biomarker disease HPO
CUI: C0040822
Disease: Tremor
Tremor 		0.100 Biomarker phenotype HPO
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		0.100 Biomarker phenotype HPO
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		0.100 Biomarker disease HPO
CUI: C0241355
Disease: Small testicle
Small testicle 		0.100 Biomarker phenotype HPO
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast 		0.100 Biomarker disease HPO
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.100 Biomarker disease HPO
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		0.100 Biomarker disease HPO
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		0.100 Biomarker disease HPO
CUI: C0520927
Disease: Decreased fertility
Decreased fertility 		0.100 Biomarker phenotype HPO
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		0.100 Biomarker phenotype HPO
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		0.100 Biomarker group HPO
CUI: C1384606
Disease: Dyspareunia
Dyspareunia 		0.100 Biomarker phenotype HPO
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		0.100 Biomarker disease HPO
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		0.100 Biomarker disease HPO
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair 		0.100 Biomarker phenotype HPO
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair 		0.100 Biomarker phenotype HPO
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		0.100 Biomarker phenotype HPO
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired 		0.100 Biomarker phenotype HPO
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		0.100 Biomarker phenotype HPO
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		0.100 Biomarker phenotype HPO
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate 		0.100 Biomarker phenotype HPO
CUI: C4017302
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 22 WITH ANOSMIA 		0.100 CausalMutation disease CLINVAR