Long clavicles
Symptom Information:
Symptom ID: | HPO:0000890 | |||
Synonyms: |
|
|||
Quality: | ||||
Cross references: |
|
|||
Is a (Direct Parents): |
|
|||
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) Abnormality of the clavicle(HPO:0000889) Long clavicles(HPO:0000890) MedDRA: |
|||
Database Frequency: | 13 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Fibrochondrogenesis | (Orphanet:2021) |
Greenberg dysplasia | (Orphanet:1426) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Pelviscapular dysplasia | (Orphanet:93333) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
Schinzel-Giedion syndrome | (Orphanet:798) |