Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2
Gene Symbol: A2M
A2M
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0.100 SusceptibilityMutation CLINVAR

Entrez Id: 2
Gene Symbol: A2M
A2M
CUI: C1865903
Disease: Long-tract signs
Long-tract signs 		0.100 Biomarker HPO

Entrez Id: 2
Gene Symbol: A2M
A2M
CUI: C4703620
Disease: Decreased level of GABA in serum
Decreased level of GABA in serum 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0013362
Disease: Dysarthria
Dysarthria 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0024236
Disease: Lymphedema
Lymphedema 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0028738
Disease: Nystagmus
Nystagmus 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0033377
Disease: Ptosis
Ptosis 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		0.100 Biomarker HPO

Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic 		0.100 Biomarker HPO