Disease #01149 (OPSMD (opsismodysplasia (OPSMD)), OMIM:258480)

Official abbreviation OPSMD
Name opsismodysplasia (OPSMD)
OMIM ID 258480
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene INPPL1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-09-29 15:46:56 +02:00 (CEST)


Individuals

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00359405 Pat42 PubMed: Silveira 2021, Journal: Silveira 2021 - M yes Brazil - - - - - OPSMD - - INPPL1 1 1 Maria Dora Jazmin Lacarrubba-Flores
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