Disease #04454 (DRS2 (Robinow, autosomal dominant syndrome, type 2 (DRS2)), OMIM:616331)

Official abbreviation DRS2
Name Robinow, autosomal dominant syndrome, type 2 (DRS2)
OMIM ID 616331
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene DVL1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00413455 patient PubMed: Hu 2022 - ? no China - - - - - DRS2 Developmental delay, protruding forehead, hypertelorism, depressed nasal bridge, thick upper lip, mildly high palatal arch, abnormal alveolar dysplasia, curled tragus, and slightly lower ear position . Limited hip extension of both lower extremities Low weight (Z‐score − 1.49), short stature (Z‐score − 2.36). - DVL1 1 1 Juliana Mazzeu
00435229 Pat10 PubMed: Tsai 2023 - M - - - - - - - DRS2 - - DVL1 1 1 Juliana Mazzeu
00452267 patient PubMed: Smith 2024, Journal: Smith 2024 - M - United States - - - - - DRS2 macrocephaly Short stature heart defect - DVL1 1 1 Juliana Mazzeu
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