Disease #00376 (SRTD5 (dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5)), OMIM:614376)
Official abbreviation |
SRTD5 |
Name |
dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5) |
OMIM ID |
614376 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
WDR19 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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