Abnormality of the neck
Symptom Information:
Symptom ID: | HPO:0000464 | ||||||
Synonyms: |
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Quality: | |||||||
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) MedDRA: |
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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) |