Disease #06475 (NEDEHCC (Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum), OMIM:618090)

Official abbreviation NEDEHCC
Name Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum
OMIM ID 618090
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease -
Associated with 1 gene KIAA1715
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00412451 - - - - - - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412510 - - - - no - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412511 - - - - yes - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412512 - - - - yes - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412513 - - - - yes - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412514 - - - - yes - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
00412515 - - - - yes - - - - - - NEDEHCC - KIAA1715 KIAA1715 1 1 Andrea Accogli
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