Disease #06316 (SEDKF (dysplasia, spondyloepiphyseal, Kondo-Fu type), OMIM:618392)

Official abbreviation SEDKF
Name dysplasia, spondyloepiphyseal, Kondo-Fu type
OMIM ID 618392
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MBTPS1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2026-03-20 09:29:23 +01:00 (CET)


Individuals

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00465602 - PubMed: Lucas-Castro 2026, Journal: Lucas-Castro 2026 - M no Spain - - - - - SEDKF see paper; ..., 28wg-premature birth, weight 990g; 20y-height 113.5 cm, weight 26kg; pectus carinatum, protuberant abdomen, inguinal hernia, joint hypermobility, pes planus, cutis laxa, retromicrognathia; large ears, abnormal ears; cataract; craniosynostosis, no brachydactyly, genu valgo, valgus bowing tibia, hip dysplasia, kyphoscoliosis, osteopenia, spondyloepiphyseal dysplasia, no developmental delay, motor delay, no seizures MBTPS1 MBTPS1 2 1 Elsa Lucas Castro
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