(Q3508565)
English
ABCD syndrome
Autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB)
- ALBINISM, BLACK LOCK, CELL MIGRATION DISORDER OF THE NEUROCYTES OF THE GUT, AND DEAFNESS
- albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness
- ABCDS
Statements
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Identifiers
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Sitelinks
Wikipedia(6 entries)
- arwiki متلازمة إيه بي سي دي
- enwiki ABCD syndrome
- eswiki Síndrome ABCD
- frwiki Syndrome ABCD
- itwiki Sindrome ABCD
- srwiki АБЦД синдром