Disease #02878 (SCDO3 (dysostosis, spondylocostal, autosomal recessive, type 3 (SCDO-3)), OMIM:609813)

Official abbreviation SCDO3
Name dysostosis, spondylocostal, autosomal recessive, type 3 (SCDO-3)
OMIM ID 609813
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene LFNG
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)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00427959 - - - F no Algeria - 00y01m - - - SCDO3 Polyhydramnios HP:0001561 Respiratory distress HP:0002098 Kyphoscoliosis HP:0002751 Rib fusion HP:0000902 Hemivertebrae HP:0002937 Thoracic dysplasia HP:0006644 Pulmonary hypoplasia HP:0002089 Absent/hypoplastic coccyx HP:0008436 - LFNG 2 1 Edoardo Errichiello
00427960 - - - F no Italy - - - - - SCDO3 Respiratory distress HP:0002098 Hemivertebrae HP:0002937 Vertebral fusion HP:0002948 - LFNG 2 1 Edoardo Errichiello
00427961 - - - F yes Morocco - - - - - SCDO3 Spinal dysraphism HP:0010301 Hemivertebrae HP:0002937 Rib fusion HP:0000902 Short stature HP:0004322 Pectus carinatum HP:0000768 Butterfly vertebrae HP:0003316 Pulmonary hypoplasia HP:0002089 - LFNG 1 1 Edoardo Errichiello
00431334 - - 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Costa Rica - - - - - SCDO3 Short stature (10th to 25th %), vertebral segmental defects and rib fusions (9 right ribs and 10 left), left 38-degree scoliosis at L1/S1, 44-degree lordosis at L1/S1, and 32-degree kyphosis at T2/T12. LFNG LFNG 2 1 Parker Cole Wengryn
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