Disease #04652 (MCPH14 (microcephaly?, type 14, primary, autosomal recessive (MCPH-14)), OMIM:616402)

Official abbreviation MCPH14
Name microcephaly?, type 14, primary, autosomal recessive (MCPH-14)
OMIM ID 616402
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 SASS6
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095114 - - - - ? - - - - Yes - MCPH14 Congenital microcephaly - SASS6 1 1 Karen Stals
00373380 161594 - - F ? Germany - - - - - MCPH14 Microcephaly, Pachygyria, Lissencephaly SASS6 - - 1 Andreas Laner
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