Disease #01013 (MCPHA (microcephaly, Amish type (MCPHA)), OMIM:607196)

Official abbreviation MCPHA
Name microcephaly, Amish type (MCPHA)
OMIM ID 607196
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC25A19
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00213102 12185364-Fams PubMed: Rosenberg 2002 23 nuclear families connected to a single ancestral couple, 16 affected F;M yes United States Amish - - - - MCPHA see paper; ... SLC25A19 SLC25A19 1 16 Johan den Dunnen
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