Abnormality of the thorax
Symptom Information:
Symptom ID: | HPO:0000765 | ||||
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 axial skeleton morphology(HPO:0009121) Abnormality of the thorax(HPO:0000765) MedDRA: |
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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) |