Down-sloping shoulders
Symptom Information:
Symptom ID: | HPO:0200021 | |||||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of the shoulder(HPO:0003043) Down-sloping shoulders(HPO:0200021) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the thorax(HPO:0000765) Abnormality of the shoulder(HPO:0003043) Down-sloping shoulders(HPO:0200021) MedDRA: |
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Database Frequency: | 18 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
CHARGE syndrome | (Orphanet:138) |
Congenitally short costocoracoid ligament | (Orphanet:2391) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Gordon syndrome | (Orphanet:376) |
Gorlin syndrome | (Orphanet:377) |
Grant syndrome | (Orphanet:2097) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
MICROPHTHALMIA, SYNDROMIC 1 | (OMIM:309800) |
OTOFACIOCERVICAL SYNDROME 1 | (OMIM:166780) |
Otofaciocervical syndrome | (Orphanet:2792) |
RUIJS-AALFS SYNDROME | (OMIM:616200) |
Williams syndrome | (Orphanet:904) |