Redundant neck skin

Symptom Information:

Symptom ID: HPO:0005989
Synonyms:
Redundant skin folds of neck [HPO:0005989]
Redundant skin over the neck [HPO:0005989]
Redundant nuchal skin [Orphanet:14450]
Redundant neck skin [OMIM:Redundant neck skin]
Redundant skin folds of neck [OMIM:Redundant skin folds of neck]
Redundant skin over the neck [OMIM:Redundant skin over the neck]
Excess nuchal skin without pterygium colli [Orphanet:14450]
Quality:
Cross references:
HPO:0000474 "Thickened nuchal skin fold" [Orphanet:14450]
Orphanet:14450 "Excess nuchal skin without pterygium colli" [Orphanet:14450]
OMIM: "Redundant neck skin" [OMIM:Redundant neck skin]
OMIM: "Redundant skin folds of neck" [OMIM:Redundant skin folds of neck]
OMIM: "Redundant skin over the neck" [OMIM:Redundant skin over the neck]
Is a (Direct Parents):
HPO         Redundant skin
Orphanet Abnormality of the neck
HPO         Abnormality of the neck
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)
                               Redundant neck skin(HPO:0005989)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the neck(HPO:0000464)
             Redundant neck skin(HPO:0005989)
MedDRA:
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)