MedGen Find_IDs Find_Terms Annotation
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created at 2024-09-19 07:43:07 UTC
updated at 2024-09-23 18:19:38 UTC
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
622,528 entries

There is 0 pattern entry.

Label
Id
ABCDS C1838099
ABCD SYNDROME C1838099
ABCD syndrome C1838099
Albinism, Black lock, Cell migration disorder of the neurocytes of the gut and Deafness C1838099
ALBINISM, BLACK LOCK, CELL MIGRATION DISORDER OF THE NEUROCYTES OF THE GUT, AND DEAFNESS C1838099
Albinism, Black lock, Cell migration disorder of the neurocytes of the gut, and Deafness C1838099
albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness C1838099
albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness C1838099
Albinism-black lock-cell migration disorder of the neurocytes of the gut-sensorineural deafness syndrome C1838099
Albinism-black lock-cell migration disorder of the neurocytes of the gut-sensorineural hearing loss syndrome C1838099
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