Redundant neck skin
Symptom Information:
Symptom ID: | HPO:0005989 | |||||||
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 head or neck(HPO:0000152) Abnormality of the neck(HPO:0000464) Redundant neck skin(HPO:0005989) 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) Redundant neck skin(HPO:0005989) MedDRA: |
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Database Frequency: | 40 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Achondrogenesis type 1B | (Orphanet:93298) |
Achondrogenesis type 2 | (Orphanet:93296) |
Acrocephalosyndactyly | (Orphanet:946) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Costello syndrome | (Orphanet:3071) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Cutis laxa | (Orphanet:209) |
Distal trisomy 18q | (Orphanet:1716) |
Down syndrome | (Orphanet:870) |
Dysmorphism - cleft palate - loose skin | (Orphanet:1779) |
Fetal hydantoin syndrome | (Orphanet:1912) |
Fryns syndrome | (Orphanet:2059) |
Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Leprechaunism | (Orphanet:508) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephaly - seizures - intellectual deficit - heart disease | (Orphanet:2519) |
Monosomy 18p | (Orphanet:1598) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pyknoachondrogenesis | (Orphanet:3003) |
SCARF syndrome | (Orphanet:3134) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Toriello-Carey syndrome | (Orphanet:3338) |
Trisomy 12p | (Orphanet:1699) |
Velo-facial-skeletal syndrome | (Orphanet:3424) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
Zellweger syndrome | (Orphanet:912) |