Down-sloping shoulders

Symptom Information:

Symptom ID: HPO:0200021
Synonyms:
Rounded shoulders [HPO:0200021]
Rounded, sloping shoulders [HPO:0200021]
Sloping shoulders [HPO:0200021]
Sloping shoulders [Orphanet:15080]
Down-sloping shoulders [OMIM:Down-sloping shoulders]
Rounded, sloping shoulders [OMIM:Rounded, sloping shoulders]
Sloping shoulders [OMIM:Sloping shoulders]
Narrow/sloping shoulders [Orphanet:15080]
Narrow sloping shoulders [OMIM:Narrow sloping shoulders]
Round shoulders [OMIM:Round shoulders]
Narrow shoulder [Orphanet:15080]
Quality:
Cross references:
Orphanet:15080 "Narrow/sloping shoulders" [Orphanet:15080]
OMIM: "Down-sloping shoulders" [OMIM:Down-sloping shoulders]
OMIM: "Rounded, sloping shoulders" [OMIM:Rounded, sloping shoulders]
OMIM: "Sloping shoulders" [OMIM:Sloping shoulders]
OMIM: "Narrow sloping shoulders" [OMIM:Narrow sloping shoulders]
OMIM: "Round shoulders" [OMIM:Round shoulders]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
Orphanet Narrow chest
HPO         Abnormality of the shoulder
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:
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)