Disease #04656 (CAID (dysrhythmia, atrial and intestinal, chronic (CAID)), OMIM:616201)

Official abbreviation CAID
Name dysrhythmia, atrial and intestinal, chronic (CAID)
OMIM ID 616201
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SGOL1
Associated tissues -
Disease features no cognitive delay; growth retardation; no neuropsychiatric behaviors; no microcephaly; craniofacial dysmorphia; no cleft/arched palate; no syndactyly; organ abnormalitie; cardiac defects; no limb reductions; no hearing loss; skin pigmentation abnormalities; no elevated cancer incidence; no bone marrow/hematopoietic defects
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2023-08-31 23:33:06 +02:00 (CEST)

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