Disease #05189 (MEHMO;MRXS20;MRXS25 (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (MEHMO)), OMIM:300148)

Official abbreviation MEHMO;MRXS20;MRXS25
Name mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (MEHMO)
OMIM ID 300148
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene EIF2S3
Associated tissues -
Disease features -
Remarks -
Date created 2016-10-06 23:42:30 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00081327 - - - M no Slovakia (Slovak Republic) white >05y - - - MEHMO;MRXS20;MRXS25 - EIF2S3 EIF2S3 1 1 Martina Skopkova
00081328 - - - M no Germany white 04y - - - MEHMO;MRXS20;MRXS25 - EIF2S3 EIF2S3 1 1 Martina Skopkova
00081329 - - - M no Slovakia (Slovak Republic) white >01y06m - - - MEHMO;MRXS20;MRXS25 - EIF2S3 EIF2S3 1 1 Martina Skopkova
00081330 - - - M no United States white >05y - - - MEHMO;MRXS20;MRXS25 - EIF2S3 EIF2S3 1 1 Martina Skopkova
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