About: Distal Trisomy 10q

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Distal trisomy of the long arm of chromosome 10 (10q) is characterized by pre- and postnatal growth retardation, a pattern of specific facial features, hypotonia, and developmental and psychomotor delay

Attributes	Values
rdf:type	Item
owl:sameAs	Distal Trisomy 10q
description	Distal trisomy of the long arm of chromosome 10 (10q) is characterized by pre- and postnatal growth retardation, a pattern of specific facial features, hypotonia, and developmental and psychomotor delay (en)
exact match	wds:Q5282839-9FF85A0B-7520-49FD-B176-71304C0B88C2
exact match	http://www.orpha.net/ORDO/Orphanet_96102
Mondo ID	wds:Q5282839-66C2A9A8-B2DE-4F35-854D-138D50A134A4
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0019884
Mondo ID	MONDO_0019884
rdfs:label	Distal Trisomy 10q (en) trisomie distale 10q (fr) ثلث الصبغي 10 (ar)
skos:prefLabel	Distal Trisomy 10q (en) trisomie distale 10q (fr) ثلث الصبغي 10 (ar)
name	Distal Trisomy 10q (en) trisomie distale 10q (fr) ثلث الصبغي 10 (ar)
instance of	wds:Q5282839-88B29604-5448-43AE-B765-C8AF321FF7D8 wds:Q5282839-EBA786C0-FB2C-4FA7-8560-F5F947045A58
instance of	class of disease developmental defect during embryogenesis
subclass of	wds:Q5282839-48f2789d-4736-7f98-0451-a84dea5b7e28 wds:Q5282839-7BA473ED-9496-4058-9DB8-4DB71472BB71 wds:Q5282839-97F9499C-6EAC-465E-9575-DE930FAA84B9
subclass of	chromosomal anomaly with cataract chromosome 10 anomaly trisomy 10
Orphanet ID	wds:Q5282839-b8f57fa3-40b6-610a-218c-59d182d4e827
ICD-10-CM	wds:Q5282839-4501B8EA-FDC8-4950-B425-D1D4D496C9F1
Orphanet ID	96102
ICD-10-CM	Q92.3
skos:altLabel	Distal duplication 10q (en) Distal trisomy type 10q (en) Telomeric duplication 10q (en) Trisomy 10qter (en)
UMLS CUI	wds:Q5282839-5950c6c3-4831-6dac-d30a-6e5a91ad6370 wds:Q5282839-73900fde-489c-749c-2b1f-47ec5c3c8be9 wds:Q5282839-9ee14ba1-4b50-d9e1-26b4-55f7119724c0
MeSH descriptor ID	wds:Q5282839-2b4d11c8-410d-d80c-f07c-5b503ce7028c
Microsoft Academic ID	wds:Q5282839-34A94298-B88B-4408-BF2B-5E2541C7038A wds:Q5282839-75AB7F8A-C74F-47B8-AAE7-294DF92B34E3
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C538087
Microsoft Academic ID	https://makg.org/entity/2777192312 https://makg.org/entity/2911027534
UMLS CUI	C2931728 C2931731 CL512824
MeSH descriptor ID	C538087
Microsoft Academic ID	2777192312 2911027534
WikiProjectMed ID	wds:Q5282839-5F76CB99-430C-4DFB-9DCE-93E3AA5FB7C5
WikiProjectMed ID	Distal trisomy 10q
is about of	Distal Trisomy 10q https://www.wikidata.org/wiki/Special:EntityData/Q5282839 Distal trisomy 10q https://ar.wikipedia.org/wiki/%D8%AB%D9%84%D8%AB_%D8%A7%D9%84%D8%B5%D8%A8%D8%BA%D9%8A_10
is main subject of	De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR). Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1-q26.3. Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features Distal trisomy 10q due to maternal insertional translocation (15;10): A case report and review of literature. Distal trisomy 10q and limb defects Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome
is main subject of	wds:Q51911756-4BC215D1-DA6C-4422-89FE-9756A49D4ED8 wds:Q33678590-4054374E-5054-458D-BFBB-6B607510ED5D wds:Q34998296-95607EC2-2CCE-410B-A7B1-C6E315BB918C wds:Q53225111-D167A0F3-E41E-4C87-995C-7C9BBD980378 wds:Q78377331-AE06C45D-5075-418A-9F24-1113C33E6703 wds:Q53850644-5003882A-7116-44B5-892B-1F2D9AFE4D68

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