Abnormality of the thorax

Symptom Information:

Symptom ID: HPO:0000765
Synonyms:
Thorax anomaly [Orphanet:15000]
Congenital anomaly of thorax (disorder) [Orphanet:15000]
Congenital anomaly of thorax [Orphanet:15000]
Anomalies of chest/thorax/trunk [Orphanet:15000]
Quality:
Cross references:
Orphanet:15000 "Anomalies of chest/thorax/trunk" [Orphanet:15000]
UMLS:C1285210 "Congenital anomaly of thorax" [Orphanet:15000]
Is a (Direct Parents):
HPO         Abnormal axial skeleton morphology
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)
MedDRA:
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
22q11.2 deletion syndrome (Orphanet:567)
AMENORRHEA-GALACTORRHEA SYNDROME (OMIM:104600)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
Aarskog-Scott syndrome (Orphanet:915)
Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acro-pectoral syndrome (Orphanet:85203)
Acropectorovertebral dysplasia (Orphanet:957)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Beta-thalassemia major (Orphanet:231214)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Campomelia, Cumming type (Orphanet:1318)
Childhood-onset hypophosphatasia (Orphanet:247667)
Christianson syndrome (Orphanet:85278)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Criss-cross heart (Orphanet:1461)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
FASCIAL DYSTROPHY, CONGENITAL (OMIM:228020)
Familial juvenile hypertrophy of the breast (Orphanet:180176)
Familial supernumerary nipples (Orphanet:2456)
Free sialic acid storage disease, infantile form (Orphanet:309324)
GALACTORRHEA (OMIM:230300)
GAPO syndrome (Orphanet:2067)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
HERNIA, HIATUS (OMIM:142400)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Ichthyosis-cheek-eyebrow syndrome (Orphanet:2267)
Infantile hypophosphatasia (Orphanet:247651)
Infantile myofibromatosis (Orphanet:2591)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal restrictive dermopathy (Orphanet:1662)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Mesomelic dysplasia, Savarirayan type (Orphanet:85170)
Mucolipidosis type 2 (Orphanet:576)
Mulibrey nanism (Orphanet:2576)
NEMALINE MYOPATHY 8 (OMIM:615348)
Neuroblastoma (Orphanet:635)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Osteogenesis imperfecta type 3 (Orphanet:216812)
Osteopetrosis (Orphanet:2781)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Pseudoxanthoma elasticum (Orphanet:758)
Pycnodysostosis (Orphanet:763)
Pyle disease (Orphanet:3005)
Retroperitoneal fibrosis (Orphanet:49041)
SAPHO syndrome (Orphanet:793)
SPERMATOGENIC FAILURE, X-LINKED, 1 (OMIM:305700)
Scalp-ear-nipple syndrome (Orphanet:2036)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)
Torg-Winchester syndrome (Orphanet:3460)
Werner syndrome (Orphanet:902)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)