Abnormality of the neck

Symptom Information:

Symptom ID: HPO:0000464
Synonyms:
Neck anomaly [Orphanet:14000]
Congenital anomaly of neck (disorder) [Orphanet:14000]
Congenital anomaly of neck [Orphanet:14000]
Anomalies of the neck [Orphanet:14000]
Quality:
Cross references:
Orphanet:14000 "Anomalies of the neck" [Orphanet:14000]
UMLS:C0266623 "Congenital anomaly of neck" [Orphanet:14000]
Is a (Direct Parents):
HPO         Abnormality of head or neck
HPO         Abnormality of neck blood vessel
HPO         Abnormality of lateral crico-arytenoid
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)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Benign paroxysmal tonic upgaze of childhood with ataxia (Orphanet:1179)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CERVICAL VERTEBRAE, AGENESIS OF (OMIM:214290)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Diabetic embryopathy (Orphanet:1926)
Esophageal carcinoma (Orphanet:70482)
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland (Orphanet:2239)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Gorlin syndrome (Orphanet:377)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Isolated anterior cervical hypertrichosis (Orphanet:3387)
Malakoplakia (Orphanet:556)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Mowat-Wilson syndrome (Orphanet:2152)
Odontotrichomelic syndrome (Orphanet:2723)
PAROTIDOMEGALY, HEREDITARY BILATERAL (OMIM:168800)
Proteus syndrome (Orphanet:744)
Recombinant 8 syndrome (Orphanet:96167)
Retroperitoneal fibrosis (Orphanet:49041)
Second branchial cleft anomaly (Orphanet:141022)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
Sternal cleft (Orphanet:2017)
Sternal malformation - vascular dysplasia (Orphanet:3195)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Williams syndrome (Orphanet:904)
Yunis-Varon syndrome (Orphanet:3472)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)