Short toe
Symptom Information:
Symptom ID: | HPO:0001831 | |||||||||||||||||||
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) Short digit(HPO:0011927) Short toe(HPO:0001831) Abnormality of toe(HPO:0001780) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) Aplasia/hypoplasia of the extremities(HPO:0009815) Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of toe(HPO:0001780) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) Aplasia/hypoplasia involving the skeleton(HPO:0009115) Aplasia/hypoplasia of the extremities(HPO:0009815) Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493) Aplasia/Hypoplasia involving bones of the feet(HPO:0006494) Aplasia/Hypoplasia of toe(HPO:0001991) Short toe(HPO:0001831) MedDRA: |
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Database Frequency: | 52 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
2q37 microdeletion syndrome | (Orphanet:1001) |
ADAMS-OLIVER SYNDROME 4 | (OMIM:615297) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Alström syndrome | (Orphanet:64) |
Anauxetic dysplasia | (Orphanet:93347) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachydactyly type A6 | (Orphanet:93382) |
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES | (OMIM:609441) |
Camptobrachydactyly | (Orphanet:1319) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Chondrodysplasia with joint dislocations, gPAPP type | (Orphanet:280586) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Czech dysplasia, metatarsal type | (Orphanet:137678) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
FEINGOLD SYNDROME 1 | (OMIM:164280) |
Feingold syndrome | (Orphanet:1305) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | (OMIM:242100) |
Intellectual deficit, X-linked, Vitale type | (Orphanet:85289) |
Keipert syndrome | (Orphanet:2662) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE | (OMIM:612947) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Metaphyseal chondrodysplasia, Kaitila type | (Orphanet:166038) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
Myhre syndrome | (Orphanet:2588) |
Nager syndrome | (Orphanet:245) |
OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI | (OMIM:259270) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Patent ductus arteriosus - bicuspid aortic valve - hand anomalies | (Orphanet:228190) |
Self-healing collodion baby | (Orphanet:281122) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Spondyloepiphyseal dysplasia, Cantu type | (Orphanet:163654) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
Subaortic stenosis - short stature | (Orphanet:3191) |
THAI SYMPHALANGISM SYNDROME | (OMIM:608028) |
Terminal osseous dysplasia - pigmentary defects | (Orphanet:88630) |
Tetrasomy 12p | (Orphanet:884) |
Tricho-retino-dento-digital syndrome | (Orphanet:1264) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |
Yunis-Varon syndrome | (Orphanet:3472) |