Disease #00767 (GBBB1 (Opitz GBBB syndrome, type 1, X-linked (GBBB-1)), OMIM:300000)

Official abbreviation GBBB1
Name Opitz GBBB syndrome, type 1, X-linked (GBBB-1)
OMIM ID 300000
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene MID1
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

3 entries on 1 page. Showing entries 1 - 3.
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00391499 - - - - - - - - - - - GBBB1 Malformations of ventral midline MID1 MID1 1 1 Lucia Micale
00391500 - - - - - - - - - - - GBBB1 Malformations of ventral midline MID1 MID1 1 1 Lucia Micale
00391501 - - - - - - - - - - - GBBB1 Malformations of ventral midline MID1 MID1 1 1 Lucia Micale
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