Disease #04015 (LDS5;RNHF (Loeys-Dietz syndrome, type 5 (LDS-5, Rienhoff syndrome (RNHF))), OMIM:615582)

Official abbreviation LDS5;RNHF
Name Loeys-Dietz syndrome, type 5 (LDS-5, Rienhoff syndrome (RNHF))
OMIM ID 615582
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TGFB3
Associated tissues -
Disease features hypertelorism (HP:0000316); bifid uvula (HP:0000193)/cleft palate (HP:0000175); exotropia (HP:0000577); no craniosynostosis (-HP:0001363); cervical spine instability (HP:0010646); retrognathia (HP:0000278); scoliosis (HP:0002650); club foot (HP:0001762); osteoarthritis (HP:0002758); no pneumothorax (-HP:0002107); hernia (HP:0100790); no arterial tortuosity (-HP:0005116)
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-03 17:49:07 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00080864 - PubMed: Trujillano 2017 unaffected heterozygous carrier father, mother not available - - - - - - - - LDS5;RNHF Loeys-Dietz syndrome type 5 (OMIM:615582) TGFB3 TGFB3 1 1 Daniel Trujillano
00444035 277694 - - M no ? (unknown) - - - - - LDS5;RNHF Macrocephaly, Tall stature, Pes planus, Delayed fine motor development, Expressive language delay, Cerebral white matter atrophy, Hypertelorism, Increased body weight TGFB3 TGFB3 1 1 Andreas Laner
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