Disease #05454 (SMABF1 (atrophy, muscular, spinal, with congenital bone fractures, type 1 (SMABF-1)), OMIM:616866)

Official abbreviation SMABF1
Name atrophy, muscular, spinal, with congenital bone fractures, type 1 (SMABF-1)
OMIM ID 616866
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene TRIP4
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2018-07-09 15:53:18 +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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00261360 1179497 - submitted for publication M yes Saudi Arabia - - - - - SMABF1 - TRIP4 TRIP4 1 1 Anett Marais
00373743 - - - F no Greece - - - - - SMABF1 - TRIP4 TRIP4 1 1 Anett Marais
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