Narrow chest

Symptom Information:

Symptom ID: HPO:0000774
Synonyms:
Low chest circumference [HPO:0000774]
Narrow shoulders [HPO:0000774]
Narrow thorax [HPO:0000774]
Reduced anterior-posterior chest diameter [HPO:0000774]
Narrow rib cage [Orphanet:15160]
Narrow thorax (finding) [Orphanet:15160]
Narrow thorax [Orphanet:15160]
Low chest circumference [OMIM:Low chest circumference]
Narrow chest [OMIM:Narrow chest]
Narrow shoulders [OMIM:Narrow shoulders]
Narrow thorax [OMIM:Narrow thorax]
Reduced anterior-posterior chest diameter [OMIM:Reduced anterior-posterior chest diameter]
Narrow rib cage/thorax [Orphanet:15160]
Narrow chest (in some patients) [OMIM:Narrow chest (in some patients)]
Narrow shoulders (1 patient) [OMIM:Narrow shoulders (1 patient)]
Narrow/sloping shoulders [Orphanet:15080]
Narrow shoulder [Orphanet:15080]
Quality:
Cross references:
Orphanet:15160 "Narrow rib cage/thorax" [Orphanet:15160]
Orphanet:15080 "Narrow/sloping shoulders" [Orphanet:15080]
OMIM: "Low chest circumference" [OMIM:Low chest circumference]
OMIM: "Narrow chest" [OMIM:Narrow chest]
OMIM: "Narrow shoulders" [OMIM:Narrow shoulders]
OMIM: "Narrow thorax" [OMIM:Narrow thorax]
OMIM: "Reduced anterior-posterior chest diameter" [OMIM:Reduced anterior-posterior chest diameter]
OMIM: "Narrow chest (in some patients)" [OMIM:Narrow chest (in some patients)]
OMIM: "Narrow shoulders (1 patient)" [OMIM:Narrow shoulders (1 patient)]
UMLS:C0426790 "Narrow thorax" [Orphanet:15160]
Is a (Direct Parents):
HPO         Thoracic hypoplasia
Orphanet Abnormality of the thorax
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 axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Thoracic hypoplasia(HPO:0005257)
                      Narrow chest(HPO:0000774)
MedDRA:
Database Frequency: 167 / 7739
Resource:

All diseases associated with this symptom:

3q13 microdeletion syndrome (Orphanet:1621)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES (OMIM:208081)
Achondrogenesis (Orphanet:932)
Achondrogenesis type 1A (Orphanet:93299)
Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
Achondroplasia (Orphanet:15)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocapitofemoral dysplasia (Orphanet:63446)
Antley-Bixler syndrome (Orphanet:83)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Atelosteogenesis type I (Orphanet:1190)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Blackfan-Diamond anemia (Orphanet:124)
Bohring-Opitz syndrome (Orphanet:97297)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
Boomerang dysplasia (Orphanet:1263)
Brachydactyly - mesomelia - intellectual deficit - heart defects (Orphanet:1277)
Brachydactyly-long thumb syndrome (Orphanet:2946)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CLAPO syndrome (Orphanet:168984)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Campomelic dysplasia (Orphanet:140)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Christianson syndrome (Orphanet:85278)
Cleidocranial dysplasia (Orphanet:1452)
Cloverleaf skull - multiple congenital anomalies (Orphanet:93267)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Congenitally short costocoracoid ligament (Orphanet:2391)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniomicromelic syndrome (Orphanet:1524)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
DIAMOND-BLACKFAN ANEMIA 1 (OMIM:105650)
Desbuquois syndrome (Orphanet:1425)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Dysosteosclerosis (Orphanet:1782)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ehlers-Danlos syndrome type 11 (Orphanet:2295)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ellis Van Creveld syndrome (Orphanet:289)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
Familial visceral myopathy (Orphanet:2604)
Fibrochondrogenesis (Orphanet:2021)
Fryns syndrome (Orphanet:2059)
Goldblatt syndrome (Orphanet:166272)
Grant syndrome (Orphanet:2097)
Greenberg dysplasia (Orphanet:1426)
Harrod syndrome (Orphanet:2115)
Heart defects - limb shortening (Orphanet:1354)
Heart-hand syndrome type 2 (Orphanet:1350)
Hennekam syndrome (Orphanet:2136)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Holt-Oram syndrome (Orphanet:392)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypophosphatasia (Orphanet:436)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Jeune syndrome (Orphanet:474)
Kyphomelic dysplasia (Orphanet:1801)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lethal Larsen-like syndrome (Orphanet:2371)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal recessive chondrodysplasia (Orphanet:1423)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
MENTAL RETARDATION, X-LINKED 90 (OMIM:300850)
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 (OMIM:300676)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MYASTHENIC SYNDROME, CONGENITAL, 8 (OMIM:615120)
Menkes disease (Orphanet:565)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Metatropic dysplasia (Orphanet:2635)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Micromelic dwarfism, Fryns type (Orphanet:2641)
Microphthalmia, Lenz type (Orphanet:568)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mulibrey nanism (Orphanet:2576)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
NEMALINE MYOPATHY 9 (OMIM:615731)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephronophthisis 9 (OMIM:613824)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Night blindness - skeletal anomalies - dysmorphism (Orphanet:1390)
Non-distal trisomy 13q (Orphanet:1702)
OSTEOGENESIS IMPERFECTA, TYPE VII (OMIM:610682)
OSTEOGENESIS IMPERFECTA, TYPE X (OMIM:613848)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Occipital horn syndrome (Orphanet:198)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Opsismodysplasia (Orphanet:2746)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta (Orphanet:666)
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism (Orphanet:91133)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Platyspondylic dysplasia, Torrance type (Orphanet:85166)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Pycnodysostosis (Orphanet:763)
Ruvalcaba syndrome (Orphanet:3121)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB (OMIM:615087)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE III (OMIM:263510)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
Schneckenbecken dysplasia (Orphanet:3144)
Severe achondroplasia - developmental delay - acanthosis nigricans (Orphanet:85165)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Short stature, Brussels type (Orphanet:2867)
Short-rib thoracic dysplasia 11 with or without polydactyly (OMIM:615633)
Short-rib thoracic dysplasia 13 with or without polydactyly (OMIM:616300)
Short-rib thoracic dysplasia 2 with or without polydactyly (OMIM:611263)
Short-rib thoracic dysplasia 4 with or without polydactyly (OMIM:613819)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Short-rib thoracic dysplasia 7 with or without polydactyly (OMIM:614091)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Shwachman-Diamond syndrome (Orphanet:811)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Sprengel deformity (Orphanet:3181)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Thoracic dysplasia-hydrocephalus syndrome (Orphanet:1861)
Thoracomelic dysplasia (Orphanet:1803)
Triploidy (Orphanet:3376)
Trisomy 13 (Orphanet:3378)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
Williams syndrome (Orphanet:904)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Yunis-Varon syndrome (Orphanet:3472)