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  Diseases matching the query *Ehlers-Danlos* and the corresponding human biomolecules involved in at least one interaction

Primary Hits

Found inDisease identifierOMIM identifierDisease nameNumber of biomolecules
DI-00435130070Ehlers-Danlos syndrome with short stature and limb anomalies1Show list of biomolecules +1
DI-00436130000Ehlers-Danlos syndrome, classic type3Show list of biomolecules +3
DI-00438130020Ehlers-Danlos syndrome 31Show list of biomolecules +1
DI-00439130050Ehlers-Danlos syndrome 41Show list of biomolecules +1
DI-00440225400Ehlers-Danlos syndrome 61Show list of biomolecules +1
DI-00442130060Ehlers-Danlos syndrome 7A1Show list of biomolecules +1
DI-00443130060Ehlers-Danlos syndrome 7B1Show list of biomolecules +1
DI-00444225410Ehlers-Danlos syndrome 7C1Show list of biomolecules +1
DI-01097606408Ehlers-Danlos syndrome due to tenascin X deficiency1Show list of biomolecules +1
DI-01317225320Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form1Show list of biomolecules +1
DI-03408614557Ehlers-Danlos syndrome, with progressive kyphoscoliosis, myopathy, and hearing loss1Show list of biomolecules +1
DI-04848130080Ehlers-Danlos syndrome, periodontal type, 11Show list of biomolecules +1
DI-04849617174Ehlers-Danlos syndrome, periodontal type, 21Show list of biomolecules +1
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Secondary Hits

No match found