Disease #05181 (SPATCCM (tetraplegia, spastic, thin corpus callosum, and progressive microcephaly (SPATCCM)), OMIM:616657)

Official abbreviation SPATCCM
Name tetraplegia, spastic, thin corpus callosum, and progressive microcephaly (SPATCCM)
OMIM ID 616657
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 SLC1A4
Associated tissues -
Disease features -
Remarks -
Date created 2016-09-13 16:05:04 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080826 - PubMed: Trujillano 2017 no information from parents - - - - - - - - SPATCCM Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (OMIM:616657) SLC1A4 SLC1A4 1 1 Daniel Trujillano
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