Hammertoe
Symptom Information:
Symptom ID: | HPO:0001765 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Abnormality of toe(HPO:0001780) Hammertoe(HPO:0001765) Abnormality of digit(HPO:0011297) Abnormality of toe(HPO:0001780) Hammertoe(HPO:0001765) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Extremity deformities(MedDRA:10012139) Hammertoe(HPO:0001765) |
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Database Frequency: | 63 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q11 microdeletion syndrome | (Orphanet:97685) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES | (OMIM:208080) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Autosomal dominant Charcot-Marie-Tooth disease type 2D | (Orphanet:99938) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | (Orphanet:209341) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F | (Orphanet:352670) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive cerebelloparenchymal disorder type 3 | (Orphanet:1170) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Bifunctional enzyme deficiency | (Orphanet:300) |
CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA | (OMIM:211930) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
Craniosynostosis and dental anomalies | (Orphanet:284149) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Distal hereditary motor neuropathy type 1 | (Orphanet:139518) |
Distal hereditary motor neuropathy type 5 | (Orphanet:139536) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Friedreich ataxia 2 | (OMIM:601992) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Isolated plagiocephaly | (Orphanet:35098) |
Lower motor neuron syndrome with late-adult onset | (Orphanet:276435) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 | (OMIM:614563) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 | (OMIM:611091) |
MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC | (OMIM:616040) |
Marfan syndrome type 1 | (Orphanet:284963) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID | (OMIM:615575) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Short-rib thoracic dysplasia 5 with or without polydactyly | (OMIM:614376) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
Young adult-onset distal hereditary motor neuropathy | (Orphanet:314485) |