Redundant skin

Symptom Information:

Symptom ID: HPO:0001582
Synonyms:
Loose redundant skin [HPO:0001582]
Redundant skin folds [HPO:0001582]
Sagging, redundant skin [HPO:0001582]
Loose skin folds [Orphanet:23470]
Cutis Laxa [Orphanet:23470]
Excessive skin [Orphanet:23470]
Loose redundant skin [OMIM:Loose redundant skin]
Redundant skin [OMIM:Redundant skin]
Redundant skin folds [OMIM:Redundant skin folds]
Sagging, redundant skin [OMIM:Sagging, redundant skin]
Loose skin/skin relaxation/excess skin/creases [Orphanet:23470]
Cutis laxa [Orphanet:23470]
Excessive skin [MedDRA:10064503]
Cutis laxa [MedDRA:10011692]
Dermatochalasis [MedDRA:10011692]
Dermatolysis [MedDRA:10011692]
Skin laxity [MedDRA:10011692]
Cutis laxa (especially hands and feet) [OMIM:Cutis laxa (especially hands and feet)]
Cutis laxa (infancy) [OMIM:Cutis laxa (infancy)]
Loose redundant skin (especially of dorsum of hands and feet and anterior abdominal wall) [OMIM:Loose redundant skin (especially of dorsum of hands and feet and anterior abdominal wall)]
Loose, redundant skin [OMIM:Loose, redundant skin]
Quality:
Cross references:
HPO:0000973 "Cutis laxa" [Orphanet:23470]
Orphanet:23470 "Loose skin/skin relaxation/excess skin/creases" [Orphanet:23470]
OMIM: "Loose redundant skin" [OMIM:Loose redundant skin]
OMIM: "Redundant skin" [OMIM:Redundant skin]
OMIM: "Redundant skin folds" [OMIM:Redundant skin folds]
OMIM: "Sagging, redundant skin" [OMIM:Sagging, redundant skin]
OMIM: "Cutis laxa (especially hands and feet)" [OMIM:Cutis laxa (especially hands and feet)]
OMIM: "Cutis laxa (infancy)" [OMIM:Cutis laxa (infancy)]
OMIM: "Loose redundant skin (especially of dorsum of hands and feet and anterior abdominal wall)" [OMIM:Loose redundant skin (especially of dorsum of hands and feet and anterior abdominal wall)]
OMIM: "Loose, redundant skin" [OMIM:Loose, redundant skin]
UMLS:C0010495 "Cutis Laxa" [Orphanet:23470]
UMLS:C1399774 "Excessive skin" [Orphanet:23470]
Is a (Direct Parents):
HPO         Cutis laxa
MedDRA Dermal and epidermal conditions NEC
MedDRA Connective tissue disorders (excl LE)
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormal elasticity of skin(HPO:0010647)
                      Abnormally lax or hyperextensible skin(HPO:0008067)
                         Cutis laxa(HPO:0000973)
                            Redundant skin(HPO:0001582)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Dermal and epidermal conditions NEC(MedDRA:10012424)
          Redundant skin(HPO:0001582)
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Connective tissue disorders (excl congenital)(MedDRA:10010761)
       Connective tissue disorders (excl LE)(MedDRA:10010762)
          Redundant skin(HPO:0001582)
Database Frequency: 51 / 7739
Resource:

All diseases associated with this symptom:

6p22 microdeletion syndrome (Orphanet:251046)
Ablepharon macrostomia syndrome (Orphanet:920)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal dominant cutis laxa (Orphanet:90348)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Autosomal recessive cutis laxa type 2 (Orphanet:90350)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
Axenfeld-Rieger syndrome (Orphanet:782)
Barber-Say syndrome (Orphanet:1231)
Beckwith-Wiedemann syndrome (Orphanet:116)
Blepharonasofacial malformation syndrome (Orphanet:1252)
C syndrome (Orphanet:1308)
CUTIS LAXA, AUTOSOMAL DOMINANT 1 (OMIM:123700)
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Coffin-Lowry syndrome (Orphanet:192)
Costello syndrome (Orphanet:3071)
Cranio-osteoarthropathy (Orphanet:1525)
Cutis laxa (Orphanet:209)
Cutis laxa-Marfanoid syndrome (Orphanet:171719)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
De Barsy syndrome (Orphanet:2962)
Dysmorphism - cleft palate - loose skin (Orphanet:1779)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Geroderma osteodysplastica (Orphanet:2078)
Keutel syndrome (Orphanet:85202)
Langer-Giedion syndrome (Orphanet:502)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Menkes disease (Orphanet:565)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Occipital horn syndrome (Orphanet:198)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Progeroid syndrome, Petty type (Orphanet:2963)
Pseudoxanthoma elasticum (Orphanet:758)
RENAL HYPODYSPLASIA/APLASIA 2 (OMIM:615721)
Recombinant 8 syndrome (Orphanet:96167)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Transaldolase deficiency (Orphanet:101028)
Weaver syndrome (Orphanet:3447)
Williams syndrome (Orphanet:904)
Wrinkly skin syndrome (Orphanet:2834)
X-linked creatine transporter deficiency (Orphanet:52503)
Yunis-Varon syndrome (Orphanet:3472)