Long foot
Symptom Information:
Symptom ID: | HPO:0001833 | ||||||||
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 lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Long foot(HPO:0001833) MedDRA: |
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Database Frequency: | 33 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
17q11.2 microduplication syndrome | (Orphanet:139474) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
5p13 microduplication syndrome | (Orphanet:329802) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
CHROMOSOME Xq26.3 DUPLICATION SYNDROME | (OMIM:300942) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
Cohen syndrome | (Orphanet:193) |
DERMATOLEUKODYSTROPHY | (OMIM:221790) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
GIACHETI SYNDROME | (OMIM:612917) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
MENTAL RETARDATION, X-LINKED 19 | (OMIM:300844) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 | (OMIM:300676) |
MOMO syndrome | (Orphanet:2563) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Pseudoleprechaunism syndrome, Patterson type | (Orphanet:2976) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Sotos syndrome | (Orphanet:821) |
Trisomy 1q | (Orphanet:261344) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
Zechi-Ceide syndrome | (Orphanet:217017) |
Zunich-Kaye syndrome | (Orphanet:3474) |