Disease #05899 (RENS1 (Renpenning syndrome, type 1 (RENS1)), OMIM:309500)

Official abbreviation RENS1
Name Renpenning syndrome, type 1 (RENS1)
OMIM ID 309500
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PQBP1
Associated tissues -
Disease features -
Remarks -
Date created 2021-02-09 15:16:23 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00466080 337928 - - M ? Syria - - - - - RENS1 Absent speech, Intellectual disability, Pruritus, Autism, Microcephaly, Neurodevelopmental delay PQBP1 PQBP1 1 1 Andreas Laner
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