Rocker bottom foot
Symptom Information:
Symptom ID: | HPO:0001838 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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 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) |
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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) |