Broad finger
Symptom Information:
Symptom ID: | HPO:0001500 | ||||
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 appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of finger(HPO:0001167) Broad finger(HPO:0001500) Abnormality of digit(HPO:0011297) Abnormality of finger(HPO:0001167) Broad finger(HPO:0001500) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Brachydactyly type A6 | (Orphanet:93382) |
Coffin-Lowry syndrome | (Orphanet:192) |
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES | (OMIM:614684) |
Keipert syndrome | (Orphanet:2662) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nance-Horan syndrome | (Orphanet:627) |
Subaortic stenosis - short stature | (Orphanet:3191) |