Disease #03972 (SRTD8;SRPS6 (dysplasia, thoracic, short-rib, type 8 with/without polydactyly (SRTD8, short rib polydactyly syndrome 6 (SRPS6))), OMIM:615503)

Official abbreviation SRTD8;SRPS6
Name dysplasia, thoracic, short-rib, type 8 with/without polydactyly (SRTD8, short rib polydactyly syndrome 6 (SRPS6))
OMIM ID 615503
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDR60
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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