Disease #00596 (TD1 (dysplasia, thanatophoric, type I (TD1)), OMIM:187600)
Official abbreviation |
TD1 |
Name |
dysplasia, thanatophoric, type I (TD1) |
OMIM ID |
187600 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
FGFR3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-10-22 16:19:52 +02:00 (CEST) |
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