Source: ALL
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: C0234229
Disease: Deep pain
Deep pain 		1 0 1 5.3E-02 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 5.3E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 5.3E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 5.3E-02 0 0
CUI: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy 		1 0 1 5.3E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 5.3E-02 0 0
CUI: C0346363
Disease: Nevus of conjunctiva
Nevus of conjunctiva 		1 0 1 5.3E-02 0 0
CUI: C0403639
Disease: Chemical cystitis
Chemical cystitis 		1 0 1 5.3E-02 0 0
CUI: C1319183
Disease: Corticosteroid induced cataract
Corticosteroid induced cataract 		1 0 1 5.3E-02 0 0
CUI: C1697976
Disease: Hypotestosteronism
Hypotestosteronism 		1 0 1 5.3E-02 0 0
CUI: C1708341
Disease: Heavier Menses
Heavier Menses 		1 0 1 5.3E-02 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 5.3E-02 0 0
CUI: C1840391
Disease: Pseudohypoaldosteronism, Type IIc
Pseudohypoaldosteronism, Type IIc 		1 0 1 5.3E-02 0 0
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 5.3E-02 0 0
CUI: C1850395
Disease: Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive 		1 1 1 5.3E-02 1 0.50
CUI: C1858804
Disease: Cerebellar Ataxia, Deafness, and Narcolepsy
Cerebellar Ataxia, Deafness, and Narcolepsy 		1 0 1 5.3E-02 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 5.3E-02 0 0
CUI: C2751092
Disease: Neuropathy, Hereditary Sensory And Autonomic, Type IIB
Neuropathy, Hereditary Sensory And Autonomic, Type IIB 		1 0 1 5.3E-02 0 0
CUI: C3150896
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC 		1 5 1 5.3E-02 1 0.17
CUI: C3150972
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE ID
NEUROPATHY, HEREDITARY SENSORY, TYPE ID 		1 0 1 5.3E-02 0 0
CUI: C3279885
Disease: Hereditary Sensory and Autonomic Neuropathy Type Ie
Hereditary Sensory and Autonomic Neuropathy Type Ie 		1 0 1 5.3E-02 0 0
CUI: C3280168
Disease: NEUROPATHY, HEREDITARY SENSORY, TYPE IIC
NEUROPATHY, HEREDITARY SENSORY, TYPE IIC 		1 0 1 5.3E-02 0 0
CUI: C3280283
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 9
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 		1 0 1 5.3E-02 0 0
CUI: C3809882
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII 		1 0 1 5.3E-02 0 0
CUI: C3809899
Disease: EPISODIC PAIN SYNDROME, FAMILIAL, 3
EPISODIC PAIN SYNDROME, FAMILIAL, 3 		1 0 1 5.3E-02 0 0