Disease #04404 (SRTD13 (dysplasia, short-rib thoracic, type 13 with/without polydactyly (SRTD-13)), OMIM:616300)

Official abbreviation SRTD13
Name dysplasia, short-rib thoracic, type 13 with/without polydactyly (SRTD-13)
OMIM ID 616300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CEP120
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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