Ectrodactyly
Symptom Information:
Symptom ID: | HPO:0100257 | ||
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) Ectrodactyly(HPO:0100257) MedDRA: |
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Database Frequency: | 27 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ADULT syndrome | (Orphanet:978) |
ANONYCHIA-ECTRODACTYLY | (OMIM:106900) |
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME | (OMIM:612576) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
ECTRODACTYLY-CLEFT PALATE SYNDROME | (OMIM:129830) |
EEM syndrome | (Orphanet:1897) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Focal dermal hypoplasia | (Orphanet:2092) |
Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
Hypoglossia - hypodactyly | (Orphanet:989) |
Intellectual deficit - spasticity - ectrodactyly | (Orphanet:1891) |
Kallmann syndrome | (Orphanet:478) |
Karsch-Neugebauer syndrome | (Orphanet:2329) |
Limb-mammary syndrome | (Orphanet:69085) |
Moebius syndrome | (Orphanet:570) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Patterson-Stevenson-Fontaine syndrome | (Orphanet:2439) |
Phocomelia, Schinzel type | (Orphanet:2879) |
SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA | (OMIM:183500) |
SPLIT-HAND/FOOT MALFORMATION 1 | (OMIM:183600) |
SPLIT-HAND/FOOT MALFORMATION 4 | (OMIM:605289) |
SPLIT-HAND/FOOT MALFORMATION 6 | (OMIM:225300) |
Split hand - split foot - deafness | (Orphanet:71271) |
Tetramelic monodactyly | (Orphanet:2564) |