KITLG, KIT ligand, 4254

N. diseases: 249; N. variants: 23
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0024900
Disease: Mastocytosis, Bullous
Mastocytosis, Bullous 		disease Neoplasms; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.200 None 1.000 1 2010 2010
CUI: C1835039
Disease: Melanosis, Universal
Melanosis, Universal 		disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.300 None 1.000 1 2009 2009
CUI: C4225241
Disease: DEAFNESS, AUTOSOMAL DOMINANT 69
DEAFNESS, AUTOSOMAL DOMINANT 69 		disease Disease or Syndrome 1 2 0.600 moderate 1.000 1 2 2017 2017
CUI: C4706423
Disease: Familial progressive hyper and hypopigmentation
Familial progressive hyper and hypopigmentation 		disease Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
CUI: C4024859
Disease: Progressive hyperpigmentation
Progressive hyperpigmentation 		phenotype Skin and Connective Tissue Diseases Pathologic Function 1 0.100 None 0
CUI: C1840392
Disease: HYPERPIGMENTATION, FAMILIAL PROGRESSIVE
HYPERPIGMENTATION, FAMILIAL PROGRESSIVE 		disease Skin and Connective Tissue Diseases Disease or Syndrome 3 3 0.730 strong 1.000 3 3 2009 2018
CUI: C0024901
Disease: Mastocytosis, Diffuse Cutaneous
Mastocytosis, Diffuse Cutaneous 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 4 0.200 None 1.000 1 2010 2010
CUI: C2242539
Disease: Subcutaneous infection
Subcutaneous infection 		disease Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C1720811
Disease: Tumor of Rete Testis
Tumor of Rete Testis 		disease Neoplasms; Male Urogenital Diseases; Endocrine System Diseases Neoplastic Process 6 0.300 None 1.000 2 2009 2009
CUI: C0020903
Disease: Illusions
Illusions 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 6 0.010 None 1.000 1 2017 2017
CUI: C2239120
Disease: eyelids (symptom)
eyelids (symptom) 		phenotype Sign or Symptom 6 1 0.010 None 1.000 1 2018 2018
CUI: C0158995
Disease: Congenital anemia
Congenital anemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.010 None 1.000 1 1995 1995
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 7 26 0.010 None 1.000 1 1 2015 2015
CUI: C4048549
Disease: Malignant germ cell neoplasm
Malignant germ cell neoplasm 		disease Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2013 2013
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 2 0.510 limited 1.000 1 2015 2015
CUI: C0042111
Disease: Urticaria Pigmentosa
Urticaria Pigmentosa 		disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 10 2 0.010 None 1.000 1 2007 2007
CUI: C0344312
Disease: White forelock
White forelock 		phenotype Skin and Connective Tissue Diseases Finding 12 1 0.100 None 0
CUI: C0178540
Disease: Cerebral Hypoxia-Ischemia
Cerebral Hypoxia-Ischemia 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2010 2010
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		disease Skin and Connective Tissue Diseases Disease or Syndrome 13 5 0.010 None 1.000 1 1 2009 2009
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		disease Disease or Syndrome 13 12 0.100 None 0
CUI: C0009681
Disease: Anomalous pulmonary artery
Anomalous pulmonary artery 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 14 1 0.100 None 0
CUI: C0205852
Disease: Neoplasms, Embryonal and Mixed
Neoplasms, Embryonal and Mixed 		disease Neoplasms Neoplastic Process 15 0.300 None 1.000 2 2009 2009
CUI: C0751365
Disease: Cancer, Embryonal and Mixed
Cancer, Embryonal and Mixed 		disease Neoplasms Neoplastic Process 15 0.300 None 1.000 2 2009 2009
CUI: C1456687
Disease: Polio and Post-Polio Syndrome
Polio and Post-Polio Syndrome 		disease Infections Disease or Syndrome 16 1 0.010 None 1.000 1 2017 2017
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Skin and Connective Tissue Diseases Finding 17 10 0.100 None 0