Disease #02934 (DIAR4 (diarrhea, type 4, malabsorptive, congenital (DIAR-4)), OMIM:610370)

Official abbreviation DIAR4
Name diarrhea, type 4, malabsorptive, congenital (DIAR-4)
OMIM ID 610370
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 NEUROG3
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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00451661 3bINP-047 PubMed: Vela-Amieva 2024 Parents with inbreeding and consanguinity (not molecularly tested). Co-occurrence of two different monogenic diseases F yes Mexico Mexican - - - - DIAR4 Growth delay, Type 1 diabetes. Cataract, Intellectual disability, Hepatomegaly. Co-ocurrence with Wagner syndrome 1 (OMIM: 143200) NEUROG3 NEUROG3, VCAN 2 1 Miriam Erandi Reyna-Fabián
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