Abnormality of the nasopharynx

Symptom Information:

Symptom ID: HPO:0001739
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of nasopharyngeal adenoids
HPO         Abnormality of the nose
HPO         Abnormality of the pharynx
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormality of the nasopharynx(HPO:0001739)
             Abnormality of the pharynx(HPO:0000600)
                Abnormality of the nasopharynx(HPO:0001739)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Craniometaphyseal dysplasia (Orphanet:1522)
Crouzon disease (Orphanet:207)
Distal myopathy with vocal cord weakness (Orphanet:600)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Hallermann-Streiff syndrome (Orphanet:2108)
Moebius syndrome (Orphanet:570)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Okihiro syndrome (Orphanet:93293)
Osteoglophonic dwarfism (Orphanet:2645)
Roifman syndrome (Orphanet:353298)
Schinzel-Giedion syndrome (Orphanet:798)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
VACTERL/VATER association (Orphanet:887)
X-linked Opitz G/BBB syndrome (Orphanet:306597)