Oligodactyly
Symptom Information:
Symptom ID: | HPO:0012165 | ||
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 digit(HPO:0011297) Oligodactyly(HPO:0012165) MedDRA: |
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Database Frequency: | 18 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME | (OMIM:612576) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fuhrmann syndrome | (Orphanet:2854) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Lethal occipital encephalocele-skeletal dysplasia syndrome | (Orphanet:293925) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Orofaciodigital syndrome type 10 | (Orphanet:2756) |
Pallister-Hall syndrome | (Orphanet:672) |
Phocomelia, Schinzel type | (Orphanet:2879) |
ROBERTS SYNDROME | (OMIM:268300) |
Robin sequence - oligodactyly | (Orphanet:3104) |
SANTOS SYNDROME | (OMIM:613005) |
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS | (OMIM:276822) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |
XK aprosencephaly | (Orphanet:3469) |