Disease #04038 (SRTD11 (dysplasia, thoracic, short-rib, type 11 with/without polydactyly (SRTD-11)), OMIM:615633)

Official abbreviation SRTD11
Name dysplasia, thoracic, short-rib, type 11 with/without polydactyly (SRTD-11)
OMIM ID 615633
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDR34
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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