Disease #06488 (NEDMABA (Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies), OMIM:618622)

Official abbreviation NEDMABA
Name Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies
OMIM ID 618622
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 SMPD4
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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00435150 Pat1 PubMed: Aoki 2023, Journal: Aoki 2023 2-generation family, 1 affected, unaffected heterozygous parents F no Japan - - - - - NEDMABA - SMPD4 SMPD4 1 1 Mitsuko Nakashima
00435151 Pat2 PubMed: Aoki 2023, Journal: Aoki 2023 2-generation family, 1 affected, unaffected heterozygous parents M no Japan - - - - - NEDMABA - SMPD4 SMPD4 2 1 Mitsuko Nakashima
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