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: C0000729
Disease: Abdominal Cramps
Abdominal Cramps
1 0 1 0.17 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block
1 0 1 0.17 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome
1 0 1 0.17 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome
1 0 1 0.17 0 0
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
1 0 1 0.17 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor
1 0 1 0.17 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome
1 0 1 0.17 0 0
Fusion of the left and right thalami
1 0 1 0.17 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy
1 0 1 0.17 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat
1 0 1 0.17 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7
1 0 1 0.17 0 0
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
1 0 1 0.17 0 0
X-linked Dyggve-Melchior-Clausen syndrome
1 0 1 0.17 0 0
CUI: C1846437
Disease: Deformed sella turcica
Deformed sella turcica
1 0 1 0.17 0 0
CUI: C1846446
Disease: Delayed femoral head ossification
Delayed femoral head ossification
1 0 1 0.17 0 0
Multicentric femoral head ossification
1 0 1 0.17 0 0
Anomalous branches of internal carotid artery
1 1 1 0.17 1 1.00
Multicentric ossification of proximal humeral epiphyses
1 0 1 0.17 0 0
Multicentric ossification of proximal femoral epiphyses
1 0 1 0.17 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type
1 0 1 0.17 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve
1 0 1 0.17 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital
1 0 1 0.17 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11
1 0 1 0.17 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3
1 0 1 0.17 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset
1 0 1 0.17 0 0