Disease #07200 (KMD (kyphomelic dysplasia), OMIM:211350)

Official abbreviation KMD
Name kyphomelic dysplasia
OMIM ID 211350
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CTGF
Associated tissues -
Disease features -
Remarks -
Date created 2025-11-20 10:43:53 +01:00 (CET)
Date last edited N/A

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