Rocker bottom foot

Symptom Information:

Symptom ID: HPO:0001838
Synonyms:
Congenital vertical talus [HPO:0001838]
Rocker bottom feet [HPO:0001838]
Rocker-bottom feet [HPO:0001838]
Rockerbottom feet [HPO:0001838]
Rocker bottom foot [Orphanet:22080]
Congenital vertical talus (disorder) [Orphanet:22080]
Congenital convex pes valgus (disorder) [Orphanet:22080]
Flatfoot [Orphanet:22080]
Vertical talus, congenital [Orphanet:22080]
Congenital vertical talus [OMIM:Congenital vertical talus]
Rocker-bottom feet [OMIM:Rocker-bottom feet]
Vertical talus [OMIM:Vertical talus]
Pes talus [Orphanet:22080]
Pes valgus [Orphanet:22080]
Vertical talus [Orphanet:22080]
Vertical talus [MedDRA:10066242]
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]
'Rocker bottom' feet [OMIM:'Rocker bottom' feet]
'Rocker-bottom' feet [OMIM:'Rocker-bottom' feet]
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]
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]
Rocker-bottom feet (reported in 2 patients) [OMIM:Rocker-bottom feet (reported in 2 patients)]
Vertical tali [OMIM:Vertical tali]
Quality:
Cross references:
Orphanet:22080 "Pes talus" [Orphanet:22080]
OMIM: "Congenital vertical talus" [OMIM:Congenital vertical talus]
OMIM: "Rocker-bottom feet" [OMIM:Rocker-bottom feet]
OMIM: "Vertical talus" [OMIM:Vertical talus]
OMIM: "'Rocker bottom' feet" [OMIM:'Rocker bottom' feet]
OMIM: "'Rocker-bottom' feet" [OMIM:'Rocker-bottom' feet]
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: "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]
OMIM: "Rocker-bottom feet (reported in 2 patients)" [OMIM:Rocker-bottom feet (reported in 2 patients)]
OMIM: "Vertical tali" [OMIM:Vertical tali]
UMLS:C0016202 "Flatfoot" [Orphanet:22080]
UMLS:C0240912 "Vertical talus, congenital" [Orphanet:22080]
Is a (Direct Parents):
Orphanet Abnormality of the foot
HPO         Abnormality of the talus
MedDRA Extremity deformities
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
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 the tarsal bones(HPO:0001850)
                            Abnormality of the talus(HPO:0008365)
                               Rocker bottom foot(HPO:0001838)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377)
       Extremity deformities(MedDRA:10012139)
          Rocker bottom foot(HPO:0001838)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Rocker bottom foot(HPO:0001838)
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
3M syndrome (Orphanet:2616)
6q25 microdeletion syndrome (Orphanet:251056)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED (OMIM:300158)
ARTHROGRYPOSIS, DISTAL, TYPE 1A (OMIM:108120)
ARTHROGRYPOSIS, DISTAL, TYPE 1B (OMIM:614335)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES (OMIM:208080)
Antley-Bixler syndrome (Orphanet:83)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
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 2E (Orphanet:99939)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Autosomal dominant Charcot-Marie-Tooth disease type 2P (Orphanet:300319)
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
Autosomal recessive spastic paraplegia type 5A (Orphanet:100986)
Bowen-Conradi syndrome (Orphanet:1270)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
CEREBROOCULOFACIOSKELETAL SYNDROME 2 (OMIM:610756)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
COFS syndrome (Orphanet:1466)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Congenital vertical talus (Orphanet:178382)
Costello syndrome (Orphanet:3071)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniosynostosis and dental anomalies (Orphanet:284149)
DIGITOTALAR DYSMORPHISM (OMIM:126050)
Dejerine-Sottas syndrome (Orphanet:64748)
Digitotalar dysmorphism (Orphanet:1146)
Distal monosomy 6p (Orphanet:96125)
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS (OMIM:133705)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
Fine-Lubinsky syndrome (Orphanet:1272)
Freeman-Sheldon syndrome (Orphanet:2053)
Fryns syndrome (Orphanet:2059)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Gordon syndrome (Orphanet:376)
Iniencephaly (Orphanet:63259)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Isolated plagiocephaly (Orphanet:35098)
Kallmann syndrome (Orphanet:478)
Lethal restrictive dermopathy (Orphanet:1662)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
Marfan syndrome type 1 (Orphanet:284963)
Meckel syndrome, type 12 (OMIM:616258)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Monosomy 18q (Orphanet:1600)
Mosaic trisomy 9 (Orphanet:99776)
NEU-LAXOVA SYNDROME 2 (OMIM:616038)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID (OMIM:615575)
Neu-Laxova syndrome (Orphanet:2671)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteocraniostenosis (Orphanet:2763)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pitt-Hopkins syndrome (Orphanet:2896)
Roussy-Lévy syndrome (Orphanet:3115)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Schinzel-Giedion syndrome (Orphanet:798)
Sheldon-Hall syndrome (Orphanet:1147)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Trismus - pseudocamptodactyly (Orphanet:3377)
Werner syndrome (Orphanet:902)
X-linked creatine transporter deficiency (Orphanet:52503)
Young adult-onset distal hereditary motor neuropathy (Orphanet:314485)
Zellweger syndrome (Orphanet:912)