Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
41 12 25 0.28 1 2.9E-02
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism
69 4 31 0.28 1 3.8E-02
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis
16 0 16 0.22 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia
35 19 19 0.21 2 5.0E-02
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
20 0 16 0.21 0 0
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly
16 0 15 0.20 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly
35 0 18 0.20 0 0
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly
17 0 15 0.20 0 0
Absence of secondary sex characteristics
44 0 19 0.19 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
86 0 24 0.18 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly
37 0 16 0.17 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia
39 0 16 0.17 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge
47 0 17 0.17 0 0
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency
26 0 14 0.16 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly
109 0 25 0.16 0 0
Pituitary stalk interruption syndrome
16 0 12 0.16 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
47 0 16 0.15 0 0
Congenital absence of kidneys syndrome
110 0 24 0.15 0 0
Adrenocorticotropic hormone (ACTH) deficiency (disorder)
24 1 12 0.14 1 4.3E-02
CUI: C3279571
Disease: Ectopic posterior pituitary
Ectopic posterior pituitary
16 0 11 0.14 0 0
CUI: C1859775
Disease: Anterior pituitary hypoplasia
Anterior pituitary hypoplasia
18 0 11 0.14 0 0
CUI: C4022675
Disease: Increased female libido
Increased female libido
18 0 11 0.14 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height
18 0 11 0.14 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism
178 0 30 0.14 0 0
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast
38 0 13 0.13 0 0