Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1859721
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder) 		0.600 GermlineCausalMutation disease ORPHANET Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. 28317099 2018
CUI: C1859721
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder) 		0.600 GeneticVariation disease UNIPROT Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. 28317099 2018
CUI: C1859721
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)
ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder) 		0.600 Biomarker disease CTD_human