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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