Source: INFERRED

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: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
disease 0.430 None 1.000 1 1 2015 2019
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C4084843
Disease: JOUBERT SYNDROME 26
JOUBERT SYNDROME 26
disease 0.300 None 1.000 0 2 2015 2015
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
disease 0.100 None 1.000 1 1 2018 2018
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
disease 0.100 None 1.000 1 1 2018 2018
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
Abnormal form of the vertebral bodies
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1836047
Disease: Long face
Long face
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
Recurrent upper respiratory tract infection
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C0575081
Disease: Gait abnormality
Gait abnormality
group 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
Aplasia/Hypoplasia of the corpus callosum
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
Abnormality of the hypothalamus-pituitary axis
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C4021813
Disease: Oral cleft
Oral cleft
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea
phenotype 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
disease 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.100 None 0 0
Entrez Id: 23247
Gene Symbol: KIAA0556
KIAA0556
KIAA0556 0.644 0.538 1.2E-29
CUI: C3489733
Disease: Oculomotor apraxia
Oculomotor apraxia
disease 0.100 None 0 0