Disease #05063 (CHDTHP (heart defects, congential?, hamartomas of tongue, and polysyndactyly (CHDTHP)), OMIM:217085)

Official abbreviation CHDTHP
Name heart defects, congential?, hamartomas of tongue, and polysyndactyly (CHDTHP)
OMIM ID 217085
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDPCP
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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