Source: CLINVAR ×
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: C0020074
Disease: HSAN Type IV
HSAN Type IV 		1 0 1 3.0E-03 0 0
CUI: C0020488
Disease: Hypernatremia
Hypernatremia 		1 1 1 3.0E-03 1 1.6E-03
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism 		1 0 1 3.0E-03 0 0
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity 		1 0 1 3.0E-03 0 0
CUI: C0020541
Disease: Portal Hypertension
Portal Hypertension 		1 0 1 3.0E-03 0 0
CUI: C0020545
Disease: Hypertension, Renovascular
Hypertension, Renovascular 		1 0 1 3.0E-03 0 0
CUI: C0020581
Disease: Hyphema
Hyphema 		1 0 1 3.0E-03 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		1 0 1 3.0E-03 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		1 1 1 3.0E-03 1 1.6E-03
CUI: C0022107
Disease: Irritable Mood
Irritable Mood 		1 0 1 3.0E-03 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		1 0 1 3.0E-03 0 0
CUI: C0023374
Disease: Lesch-Nyhan Syndrome
Lesch-Nyhan Syndrome 		1 0 1 3.0E-03 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma 		1 0 1 3.0E-03 0 0
CUI: C0024236
Disease: Lymphedema
Lymphedema 		1 0 1 3.0E-03 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		1 0 1 3.0E-03 0 0
CUI: C0024748
Disease: alpha-Mannosidosis
alpha-Mannosidosis 		1 62 1 3.0E-03 1 1.5E-03
CUI: C0025210
Disease: Ocular melanosis
Ocular melanosis 		1 0 1 3.0E-03 0 0
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		1 0 1 3.0E-03 0 0
CUI: C0026760
Disease: Multiple Epiphyseal Dysplasia
Multiple Epiphyseal Dysplasia 		1 0 1 3.0E-03 0 0
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		1 0 1 3.0E-03 0 0
CUI: C0027809
Disease: Neurilemmoma
Neurilemmoma 		1 0 1 3.0E-03 0 0
CUI: C0027830
Disease: neurofibroma
neurofibroma 		1 0 1 3.0E-03 0 0
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1 		1 764 1 3.0E-03 2 1.5E-03
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		1 0 1 3.0E-03 0 0
CUI: C0028866
Disease: Oculomotor Nerve Paralysis
Oculomotor Nerve Paralysis 		1 0 1 3.0E-03 0 0