DISO2_YXZ Find_IDs Find_Terms Annotation
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created at 2017-12-21 11:07:44 UTC
updated at 2017-12-22 12:31:05 UTC
2 layers
520,470 entries
Label
Id
Date reference lab test sent DISO:LNC
Allelic disorder to benign hereditary chorea (118700), which is less severe DISO:OMIM
Varicose veins (reported in 1 family) DISO:OMIM
EPIDIDYMIS, APPENDIX, TORSION DISO:DXP
Torsion of appendix epididymis DISO:ICD9CM
Torsion of appendix of epididymis DISO:MTH
Torsion appy epididymis DISO:ICD9CM
Secondary axonal degeneration and regeneration DISO:OMIM
Hypoplastic lacrimal duct DISO:OMIM
Hypoplastic lacrimal duct DISO:HPO
Underdeveloped tear duct DISO:HPO
Caused by mutation in the Ras-associated protein RAB23 gene (RAB23, 606144.0001) DISO:OMIM
Most common form of autosomal dominant hereditary spastic paraplegia (accounts for 40% of SPG cases) DISO:OMIM
Can recall staff names &or faces DISO:LNC
Restricted joint mobility (shoulders, elbows, hips) DISO:OMIM