High pitched voice

Symptom Information:

Symptom ID: HPO:0001620
Synonyms:
High-pitched voice [HPO:0001620]
High pitched voice [OMIM:High pitched voice]
High-pitched voice [OMIM:High-pitched voice]
High-pitched voice (in some patients) [OMIM:High-pitched voice (in some patients)]
High-pitched voice. [OMIM:High-pitched voice.]
high pitched voice (rare) [OMIM:high pitched voice (rare)]
Quality:
Cross references:
OMIM: "High pitched voice" [OMIM:High pitched voice]
OMIM: "High-pitched voice" [OMIM:High-pitched voice]
OMIM: "High-pitched voice (in some patients)" [OMIM:High-pitched voice (in some patients)]
OMIM: "High-pitched voice." [OMIM:High-pitched voice.]
OMIM: "high pitched voice (rare)" [OMIM:high pitched voice (rare)]
Is a (Direct Parents):
HPO         Abnormality of the voice
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:
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)