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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