Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C1848201
Disease: Subcortical Band Heterotopia
Subcortical Band Heterotopia 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0424230
Disease: Motor retardation
Motor retardation 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy 		group 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0266491
Disease: Neuronal heterotopia
Neuronal heterotopia 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0151860
Disease: Acquired porencephaly
Acquired porencephaly 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		disease 0.100 None 0 0
Entrez Id: 3912
Gene Symbol: LAMB1
LAMB1 		laminin subunit beta 1 0.615 0.654 5.1E-22
CUI: C4082172
Disease: Porencephalic cyst
Porencephalic cyst 		disease 0.100 None 0 0