Disease #06276 (NEDMEHM (Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination), OMIM:618367)

Official abbreviation NEDMEHM
Name Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination
OMIM ID 618367
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MTHFS
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00436186 Fam1 PubMed: Xu 2023 2-generation family, 1 affected, unaffected heterozygous carrier parents M - China - - - - - NEDMEHM - MTHFS MTHFS 2 1 Min Peng
00436187 Fam2 PubMed: Xu 2023 2-generation family, 1 affected, unaffected heterozygous carrier parents M - China - - - - - NEDMEHM - MTHFS MTHFS 2 1 Min Peng
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