Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1859775
Disease: Anterior pituitary hypoplasia
Anterior pituitary hypoplasia
phenotype 0.400 strong 1.000 0 0 2015 2015
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
disease 0.130 None 1.000 0 0 2007 2017
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism
disease 0.110 None 1.000 0 0 2003 2003
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
disease 0.110 None 1.000 0 0 2003 2003
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease 0.110 None 1.000 0 0 2003 2003
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1859692
Disease: Decreased cervical spine mobility
Decreased cervical spine mobility
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1858430
Disease: Death in infancy
Death in infancy
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1857641
Disease: Severe postnatal growth retardation
Severe postnatal growth retardation
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1846223
Disease: Adrenal hypoplasia
Adrenal hypoplasia
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders
group 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0700201
Disease: Dyssomnias
Dyssomnias
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C1868549
Disease: Marked delay in bone age
Marked delay in bone age
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
Abnormality of the hypothalamus-pituitary axis
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C4025669
Disease: Decreased circulating ACTH level
Decreased circulating ACTH level
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C4025170
Disease: Osteoporosis of vertebrae
Osteoporosis of vertebrae
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
Abnormality of secondary sexual hair
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C4023911
Disease: Aplasia/Hypoplasia of the breasts
Aplasia/Hypoplasia of the breasts
phenotype 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C4022751
Disease: Ectopic anterior pituitary gland
Ectopic anterior pituitary gland
disease 0.100 None 0 0
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
LIM homeobox 4 0.621 0.462 1.8E-02
CUI: C4022448
Disease: Abnormal prolactin level
Abnormal prolactin level
phenotype 0.100 None 0 0