High pitched voice
Symptom Information:
Symptom ID: | HPO:0001620 | ||||||
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) Abnormality of the voice(HPO:0001608) High pitched voice(HPO:0001620) MedDRA: |
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Database Frequency: | 32 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Bloom syndrome | (Orphanet:125) |
COLE-CARPENTER SYNDROME 2 | (OMIM:616294) |
Classic multiminicore myopathy | (Orphanet:324604) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Dubowitz syndrome | (Orphanet:235) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
Geleophysic dysplasia | (Orphanet:2623) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Laron syndrome | (Orphanet:633) |
MACS syndrome | (Orphanet:217335) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type | (Orphanet:217026) |
Mulibrey nanism | (Orphanet:2576) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Pfeiffer-Palm-Teller syndrome | (Orphanet:2871) |
Primordial short stature - microdontia - opalescent and rootless teeth | (Orphanet:46658) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
SECKEL SYNDROME 2 | (OMIM:606744) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Spinocerebellar ataxia type 20 | (Orphanet:101110) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
XFE PROGEROID SYNDROME | (OMIM:610965) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |