Disease #00773 (SGBS1 (Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)), OMIM:312870)

Official abbreviation SGBS1
Name Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)
OMIM ID 312870
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GPC3
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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00060249 - - - M no Italy - - - - - SGBS1 - - GPC3 1 1 Pamela Magini
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