Disease #00276 (3M1 (3M syndrome, type 1 (3M1)), OMIM:273750)

Official abbreviation 3M1
Name 3M syndrome, type 1 (3M1)
OMIM ID 273750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene CUL7
Associated tissues -
Disease features -
Remarks -
Date created 2013-11-22 15:47:16 +01:00 (CET)
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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00004047 - PubMed: Shaheen 2014, Journal: Shaheen 2014 - M yes Saudi Arabia Arab - - - - 3M1 small and mal-aligned teeth, skin and joint laxity, and normal motor and cognitive development CUL7 CUL7 1 1 Fowzan Alkuraya
00435457 patient - - F no Poland white 03y - - - 3M1 short stature (HP:0004322) - CUL7 1 2 Katarzyna Bilińska
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