Disease #06758 (EDSCLL2 (Ehlers-Danlos syndrome, classic-like, 2), OMIM:618000)

Official abbreviation EDSCLL2
Name Ehlers-Danlos syndrome, classic-like, 2
OMIM ID 618000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene AEBP1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00427963 patient PubMed: Sanai 2023, Journal: Sanai 2023 2-generation family, 1 affected, unaffected heterozygous parents F - Japan - - - - - EDSCLL2 - - AEBP1 1 1 Tomoki Kosho
00457221 patient PubMed: Ha 2024 16-year-old female patient of Syrian descent with a clinical diagnosis of clEDS2, short stature, and premature birth; unaffected heterozygous carrier parents F no Syria - - - - - EDSCLL2 Congenital bilateral hip dislocation (HP:0008780); varicose veins (HP:0002619), short stature (HP:0004322); increased muscle fatiguability (HP:0003750); hyperextensible skin (HP:0000974); bruising susceptibility (HP:0000978); generalized joint hypermobility (HP:0002761); limb pain (HP:0009763); dry hair (HP:0011359); sparse scalp hair (HP:0002209); brittle scalp hair (HP:0004779); narrow face (HP:0000275); narrow nasal bridge (HP:0000446); thin skin (HP:0000963); cigarette-paper scars (HP:0001073); keloids (HP:0010562); increased laxity of fingers (HP:0006149); pes planus (HP:0001763); herniation of intervertebral nuclei (HP:0008441); - AEBP1, COL11A1 2 1 Deepak Subramanian
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