Abnormality of the larynx
Symptom Information:
Symptom ID: | HPO:0001600 | ||||||
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 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: |
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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) |