Redundant skin
Symptom Information:
Symptom ID: | HPO:0001582 | |||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |