Disease #05286 (LCCS11 (contraction, lethal, congenital syndrome, type 11 (LCCS-11)), OMIM:617194)

Official abbreviation LCCS11
Name contraction, lethal, congenital syndrome, type 11 (LCCS-11)
OMIM ID 617194
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene GLDN
Associated tissues -
Disease features -
Remarks -
Date created 2017-06-21 13:42:01 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00105215 Patient_1 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 2 1 Dustin Baldridge
00105216 Patient_2 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 2 1 Dustin Baldridge
00105217 Patient_3 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 2 1 Dustin Baldridge
00105218 Patient_4 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 1 1 Dustin Baldridge
00105219 Patient_5 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 1 1 Dustin Baldridge
00105220 Patient_6 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 1 1 Dustin Baldridge
00105221 Patient_8 Manuscript in submission - - - - - - - - - LCCS11 - - GLDN 2 1 Dustin Baldridge
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