Disease #05754 (EDSSPD (Ehlers-Danlos, spondylodysplastic syndrome (EDSSPD)))

Official abbreviation EDSSPD
Name Ehlers-Danlos, spondylodysplastic syndrome (EDSSPD)
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene B4GALT7
Associated tissues -
Disease features -
Remarks -
Date created 2020-05-19 18:51:25 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00428042 I-1 PubMed: Shen et al., 2022 - M no China - - - - - EDSSPD Craniofacial abnormalities, scoliosis, fifth-finger clinodactyly, restricted elbow movement, radioulnar synostosis, aclasis of right humerus and ulna B3GALT6 B3GALT6 1 1 Oumaima Nehaili
00428043 II-1 PubMed: Shen et al., 2022 - M no China - - - - - EDSSPD Craniofacial abnormalities, scoliosis, restricted elbow movement B3GALT6 B3GALT6 1 1 Oumaima Nehaili
00428044 II-2 PubMed: Shen et al., 2022 - M no China - - - - - EDSSPD Craniofacial abnormalities, scoliosis, restricted elbow movement, B3GALT6 B3GALT6 1 1 Oumaima Nehaili
00428045 III-1 PubMed: Shen et al., 2022 - F no China - - - - - EDSSPD Prominent craniofacial abnormalities, joint hypermobility, scoliosis, fifth-finger clinodactyly, restricted elbow movement, soft/doughy skin B3GALT6 B3GALT6 2 1 Oumaima Nehaili
00428046 III-2 PubMed: Shen et al., 2022 - M no China - - - - - EDSSPD Prominent craniofacial abnormalities, scoliosis, fifth-finger clinodactyly, restricted elbow movement, joint hypermobility, barrel chest, soft/doughy skin. B3GALT6 B3GALT6 2 1 Oumaima Nehaili
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