Disease #01891 (LOCS (laryngoonychocutaneous syndrome (LOCS)), OMIM:245660)

Official abbreviation LOCS
Name laryngoonychocutaneous syndrome (LOCS)
OMIM ID 245660
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LAMA3
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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00471499 - - - - no (China) - - - - - LOCS Fetal right-sided second-degree cleft lip LAMA3 LAMA3 1 1 Lizhu Chen
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