Disease #05453 (SMABF2 (atrophy, muscular, spinal, with congenital bone fractures, type 2 (SMABF2)), OMIM:616867)

Official abbreviation SMABF2
Name atrophy, muscular, spinal, with congenital bone fractures, type 2 (SMABF2)
OMIM ID 616867
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ASCC1
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2018-07-09 15:52:08 +02:00 (CEST)
Date last edited 2020-03-03 16:18:21 +01:00 (CET)


Individuals

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00373788 - - - F yes Bahrain - 00y01m - - - SMABF2 - ASCC1 ASCC1 1 1 Anett Marais
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