Abnormality of the larynx

Symptom Information:

Symptom ID: HPO:0001600
Synonyms:
Laryngeal abnormalities [HPO:0001600]
Laryngeal anomalies [HPO:0001600]
Laryngeal abnormalities [OMIM:Laryngeal abnormalities]
Laryngeal anomalies [OMIM:Laryngeal anomalies]
Quality:
Cross references:
OMIM: "Laryngeal abnormalities" [OMIM:Laryngeal abnormalities]
OMIM: "Laryngeal anomalies" [OMIM:Laryngeal anomalies]
Is a (Direct Parents):
HPO         Abnormality of cricoid cartilage
HPO         Abnormality of the upper respiratory tract
HPO         Abnormality of lateral crico-arytenoid
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of the upper respiratory tract(HPO:0002087)
                Abnormality of the larynx(HPO:0001600)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Braddock syndrome (Orphanet:52047)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
CODAS syndrome (Orphanet:1458)
Fetal Gaucher disease (Orphanet:85212)
Focal dermal hypoplasia (Orphanet:2092)
Gaucher disease type 2 (Orphanet:77260)
Hereditary angioedema type 1 (Orphanet:100050)
Hypoplasminogenemia (Orphanet:722)
Marden-Walker syndrome (Orphanet:2461)
Meckel syndrome (Orphanet:564)
Mucopolysaccharidosis type 3 (Orphanet:581)
Palmoplantar keratoderma-esophageal carcinoma syndrome (Orphanet:2198)
Rabies (Orphanet:770)
Smith-Magenis syndrome (Orphanet:819)
Toriello-Carey syndrome (Orphanet:3338)