Hammertoe

Symptom Information:

Symptom ID: HPO:0001765
Synonyms:
Hammer toe [HPO:0001765]
Hammertoes [HPO:0001765]
Hallux hammertoe [Orphanet:22580]
Hammertoe of small toe [Orphanet:22300]
Hammer Toe [Orphanet:22580]
Hammer toe [OMIM:Hammer toe]
Hammertoes [OMIM:Hammertoes]
Dorsiflexed great toe [Orphanet:22580]
Flexion deformity of toes (excluding big toe)/hammer toe/camptodactyly of toes [Orphanet:22300]
Hammer toe [Orphanet:22580]
Foot deformity [MedDRA:10061159]
Acquired deformities of toe [MedDRA:10061159]
Acquired equinovarus deformity [MedDRA:10061159]
Cavovarus deformity of foot, acquired [MedDRA:10061159]
Cavus deformity of foot, acquired [MedDRA:10061159]
Claw foot, acquired [MedDRA:10061159]
Equinus deformity of foot, acquired [MedDRA:10061159]
Fallen arches [MedDRA:10061159]
Flat feet [MedDRA:10061159]
Flat foot [MedDRA:10061159]
Foot deformity NOS [MedDRA:10061159]
Hallux malleus [MedDRA:10061159]
Hallux rigidus [MedDRA:10061159]
Hallux valgus [MedDRA:10061159]
Hallux valgus (acquired) [MedDRA:10061159]
Hallux varus (acquired) [MedDRA:10061159]
Hammer toe [MedDRA:10061159]
Other acquired calcaneus deformity [MedDRA:10061159]
Other acquired deformities of toe [MedDRA:10061159]
Other hammer toe (acquired) [MedDRA:10061159]
Pes cavus [MedDRA:10061159]
Pes planus [MedDRA:10061159]
Pes valgus [MedDRA:10061159]
Toe deformities (acquired) [MedDRA:10061159]
Toe deformities NOS [MedDRA:10061159]
Unspecified acquired deformity of toe [MedDRA:10061159]
Toe deformity [MedDRA:10061159]
Pigeon toe [MedDRA:10061159]
In-toeing [MedDRA:10061159]
Out-toeing [MedDRA:10061159]
Metatarsus primus elevatus [MedDRA:10061159]
Splayfoot [MedDRA:10061159]
Talipes valgus acquired [MedDRA:10061159]
Bunionette [MedDRA:10061159]
Flat feet (female) [OMIM:Flat feet (female)]
Foot deformities (in some patients) [OMIM:Foot deformities (in some patients)]
Foot deformities (variable) [OMIM:Foot deformities (variable)]
Hallux valgus (in some patients) [OMIM:Hallux valgus (in some patients)]
Hammer toe (2-4 toes) [OMIM:Hammer toe (2-4 toes)]
Hammer toes [OMIM:Hammer toes]
Hammertoes (in some patients) [OMIM:Hammertoes (in some patients)]
Pes cavus (1 family) [OMIM:Pes cavus (1 family)]
Pes cavus (1 patient) [OMIM:Pes cavus (1 patient)]
Pes cavus (17%) [OMIM:Pes cavus (17%)]
Pes cavus (in 1 family) [OMIM:Pes cavus (in 1 family)]
Pes cavus (in some patients) [OMIM:Pes cavus (in some patients)]
Pes cavus (less common) [OMIM:Pes cavus (less common)]
Pes cavus (uncommon) [OMIM:Pes cavus (uncommon)]
Pes planus (1 family) [OMIM:Pes planus (1 family)]
Pes planus (rare) [OMIM:Pes planus (rare)]
Pes valgus [OMIM:Pes valgus]
Quality:
Cross references:
Orphanet:22580 "Dorsiflexed great toe" [Orphanet:22580]
Orphanet:22300 "Flexion deformity of toes (excluding big toe)/hammer toe/camptodactyly of toes" [Orphanet:22300]
OMIM: "Hammer toe" [OMIM:Hammer toe]
OMIM: "Hammertoes" [OMIM:Hammertoes]
OMIM: "Flat feet (female)" [OMIM:Flat feet (female)]
OMIM: "Foot deformities (in some patients)" [OMIM:Foot deformities (in some patients)]
OMIM: "Foot deformities (variable)" [OMIM:Foot deformities (variable)]
OMIM: "Hallux valgus (in some patients)" [OMIM:Hallux valgus (in some patients)]
OMIM: "Hammer toe (2-4 toes)" [OMIM:Hammer toe (2-4 toes)]
OMIM: "Hammer toes" [OMIM:Hammer toes]
OMIM: "Hammertoes (in some patients)" [OMIM:Hammertoes (in some patients)]
OMIM: "Pes cavus (1 family)" [OMIM:Pes cavus (1 family)]
OMIM: "Pes cavus (1 patient)" [OMIM:Pes cavus (1 patient)]
OMIM: "Pes cavus (17%)" [OMIM:Pes cavus (17%)]
OMIM: "Pes cavus (in 1 family)" [OMIM:Pes cavus (in 1 family)]
OMIM: "Pes cavus (in some patients)" [OMIM:Pes cavus (in some patients)]
OMIM: "Pes cavus (less common)" [OMIM:Pes cavus (less common)]
OMIM: "Pes cavus (uncommon)" [OMIM:Pes cavus (uncommon)]
OMIM: "Pes planus (1 family)" [OMIM:Pes planus (1 family)]
OMIM: "Pes planus (rare)" [OMIM:Pes planus (rare)]
OMIM: "Pes valgus" [OMIM:Pes valgus]
UMLS:C1136179 "Hammer Toe" [Orphanet:22580]
Is a (Direct Parents):
HPO         Abnormality of toe
MedDRA Extremity deformities
Orphanet Abnormality of the hallux
Orphanet Abnormality of the foot
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)
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)