Disease #05369 (SMD (dysplasia, spondylometaphyseal (SMD)))

Official abbreviation SMD
Name dysplasia, spondylometaphyseal (SMD)
OMIM ID -
Inheritance -
Individuals reported having this disease 14
Phenotype entries for this disease 14
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2017-12-29 15:48:06 +01:00 (CET)
Date last edited N/A


Individuals

14 entries on 1 page. Showing entries 1 - 14.
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00147033 29100092-Fam1 PubMed: Lee 2017 3-generation family, affected mother and 2 sons, unaffected parents F;M - United States - - - - - SMD - FN1 FN1 1 3 Johan den Dunnen
00147034 29100092-Fam2 PubMed: Lee 2017 2-generation family, 1 affected, unaffected non-carrier parents M - United States - - - - - SMD - FN1 FN1 1 1 Johan den Dunnen
00147035 29100092-Fam3 PubMed: Lee 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Netherlands - - - - - SMD - FN1 FN1 1 1 Johan den Dunnen
00147036 29100092-Fam4 PubMed: Lee 2017 3-generation family, affected mother/daughter, unaffected parents M - United States - - - - - SMD - FN1 FN1 1 2 Johan den Dunnen
00147037 29100092-Fam5 PubMed: Lee 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Brazil - - - - - SMD - FN1 FN1 1 1 Johan den Dunnen
00147038 29100092-Fam6 PubMed: Lee 2017 2-generation family, 1 affected, unaffected non-carrier parents F - China - - - - - SMD - FN1 FN1 1 1 Johan den Dunnen
00147039 29100092-Fam7 PubMed: Lee 2017 2-generation family, 1 affected, unaffected non-carrier parents F - Canada - - - - - SMD - FN1 FN1 1 1 Johan den Dunnen
00225439 -Pat6 Journal: Burrage 2019 - F - - - - - - - SMD see paper; … TONSL TONSL 2 1 Johan den Dunnen
00225440 -Pat7-1 Journal: Burrage 2019 2-generation family, affected brother/SISTER F - - - - - - - SMD see paper; … TONSL TONSL 2 2 Johan den Dunnen
00225441 -Pat7-2 Journal: Burrage 2019 - F - - - - - - - SMD see paper; … TONSL TONSL 2 1 Johan den Dunnen
00225442 -Pat8 Journal: Burrage 2019 - F - - - - - - - SMD see paper; … TONSL TONSL 2 1 Johan den Dunnen
00418528 Fam1PatIV3 PubMed: Pagnamenta 2022 2-generation family, 3 affected brothers, unaffected heterozygous carrier parents M yes Pakistan - - - - - SMD birth weight 2700g; normal developmental milestones; <4y-normal groth/feeding; height 158.5 cm (-2.5 SD); mild rhizomelia upper and lower limbs; OFC 50-75th; mild kyphosis, thoracic region; broad thumbs, short 4-5th metacarpels; no acromelia; flat feet; normal face; normal palate; platyspondyly; (widespread metaphyseal changes; delayed bone age; normal bone density - PRKG2 1 3 Johan den Dunnen
00418529 Fam1PatIV6 PubMed: Pagnamenta 2022 brother M yes Pakistan - - - - - OI, SMD , hypotonia; normal developmental milestones; poor feeder; height 140.8 cm (-4.9 SD); moderate rhizomelia upper and lower limbs; OFC 50-75th; mild kyphosis, mid-thoracic; broad thumb; no acromelia; triangular face (when younger); multiple Wormian bones; normal palate; platyspondyly; metaphyseal changes; slender bones with thin cortices, mild bowing femur, small irregular femoral heads; multiple fractures (arm as infant, wrist aged 8y, wedge T6 vertebra), blue sclerae - COL1A1, PRKG2 2 1 Johan den Dunnen
00418530 Fam1PatIV7 PubMed: Pagnamenta 2022 brother M yes Pakistan - - - - - SMD normal developmental milestones; height 143.8 cm (-3.11 SD); mild rhizomelia upper and lower limbs; OFC 50-75th; no acromelia; mild shortening toes; normal face; normal palate; mild platyspondyly; metaphyseal changes, broadened and irregular; normal bone density - PRKG2 1 1 Johan den Dunnen
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