Showing entry for Growth/differentiation factor 5


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT010351
Protein NameGrowth/differentiation factor 5
Uniport IdP43026
GeneGDF5
Gene Id8200
DomainTGFb_propeptide; TGF_beta
Pfam PF00019   PF00688  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
3. Environmental Information Processing 3.3 Signaling molecules and interaction hsa04060 Cytokine-cytokine receptor interaction
3. Environmental Information Processing 3.2 Signal transduction hsa04350 TGF-beta signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04390 Hippo signaling pathway
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0030509 BMP signaling pathway
Biological Process GO:0007267 cell-cell signaling
Biological Process GO:0060591 chondroblast differentiation
Biological Process GO:0030326 embryonic limb morphogenesis
Biological Process GO:0035136 forelimb morphogenesis
Biological Process GO:0035137 hindlimb morphogenesis
Biological Process GO:0032331 negative regulation of chondrocyte differentiation
Biological Process GO:0050680 negative regulation of epithelial cell proliferation
Biological Process GO:2001054 negative regulation of mesenchymal cell apoptotic process
Biological Process GO:0043524 negative regulation of neuron apoptotic process
Biological Process GO:0043932 ossification involved in bone remodeling
Biological Process GO:0030513 positive regulation of BMP signaling pathway
Biological Process GO:0032332 positive regulation of chondrocyte differentiation
Biological Process GO:0045666 positive regulation of neuron differentiation
Biological Process GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
Biological Process GO:0040014 regulation of multicellular organism growth
Biological Process GO:0060390 regulation of SMAD protein signal transduction
Biological Process GO:0009612 response to mechanical stimulus
Biological Process GO:0060395 SMAD protein signal transduction
Biological Process GO:0007179 transforming growth factor beta receptor signaling pathway
molecular function GO:0036122 BMP binding
molecular function GO:0005125 cytokine activity
molecular function GO:0008083 growth factor activity
molecular function GO:0042802 identical protein binding
cellular component GO:0005576 extracellular region
cellular component GO:0005615 extracellular space
cellular component GO:0005886 plasma membrane
Reactome
Pathway Id Pathway Name
R-HSA-1474244 Extracellular matrix organization
R-HSA-1566948 Elastic fibre formation
R-HSA-2129379 Molecules associated with elastic fibres
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0003864 BXGD000231 Arthritis Musculoskeletal Diseases
C0003873 BXGD000236 Rheumatoid Arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C0004604 BXGD000278 Back Pain Pathological Conditions, Signs and Symptoms
C0005890 BXGD000345 Body Height
C0005910 BXGD000349 Body Weight Pathological Conditions, Signs and Symptoms
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0007131 BXGD000441 Non-Small Cell Lung Carcinoma Neoplasms; Respiratory Tract Diseases
C0009081 BXGD000581 Congenital clubfoot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0011854 BXGD000753 Diabetes Mellitus, Insulin-Dependent Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0016202 BXGD001050 Flatfoot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0016506 BXGD001062 Foot Deformities Musculoskeletal Diseases
C0016529 BXGD001068 Forced expiratory volume function
C0018536 BXGD001201 Hallux Valgus Musculoskeletal Diseases
C0018777 BXGD001217 Conductive hearing loss Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0019555 BXGD001334 Hip Dislocation, Congenital Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Wounds and Injuries
C0020459 BXGD001394 Hyperinsulinism Nutritional and Metabolic Diseases
C0020608 BXGD001443 Hypodontia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0024031 BXGD001727 Low Back Pain Pathological Conditions, Signs and Symptoms
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025995 BXGD001885 Micromelia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0026277 BXGD001899 Mixed Salivary Gland Tumor Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0028259 BXGD002073 Nodule
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0029408 BXGD002137 Degenerative polyarthritis Musculoskeletal Diseases
C0029410 BXGD002138 Osteoarthritis of hip Musculoskeletal Diseases
C0029422 BXGD002142 Osteochondrodysplasias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0029453 BXGD002154 Osteopenia Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0037822 BXGD002706 Speech Disorders Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0038016 BXGD002727 Spondylolisthesis Musculoskeletal Diseases
C0038017 BXGD002728 Congenital spondylolisthesis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0038018 BXGD002729 Spondylolysis Musculoskeletal Diseases
C0038379 BXGD002752 Strabismus Eye Diseases; Nervous System Diseases
C0039075 BXGD002788 Syndactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0042834 BXGD003004 Vital capacity
C0086743 BXGD003308 Osteoarthrosis Deformans Musculoskeletal Diseases
C0152427 BXGD003590 Polydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0152441 BXGD003594 Madelung Deformity Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0157946 BXGD003873 Osteoarthrosis, localized, not specified whether primary or secondary Musculoskeletal Diseases
C0158252 BXGD003877 Intervertebral disc disorder Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0158266 BXGD003878 Intervertebral Disc Degeneration Musculoskeletal Diseases
C0162298 BXGD003933 Joint stiffness Musculoskeletal Diseases
C0175700 BXGD004006 Multiple synostosis syndrome Musculoskeletal Diseases
C0205682 BXGD004105 Waist-Hip Ratio
C0206762 BXGD004290 Limb Deformities, Congenital Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221170 BXGD004400 Muscular stiffness Nervous System Diseases
C0221352 BXGD004444 Syndactyly of fingers Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases
C0221357 BXGD004449 Brachydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221775 BXGD004480 Lumbar disc disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0231679 BXGD004507 Ulnar deviation of the fingers
C0231749 BXGD004520 Knee pain Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0235833 BXGD004775 Congenital diaphragmatic hernia Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0239174 BXGD004969 Late tooth eruption
C0239399 BXGD004981 Short extremities
C0240912 BXGD005062 Vertical Talus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0263523 BXGD005320 Micronychia (disorder) Skin and Connective Tissue Diseases
C0263874 BXGD005352 Degeneration of lumbar intervertebral disc Musculoskeletal Diseases
C0265260 BXGD005488 Chondrodysplasia, Grebe type Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0265642 BXGD005557 Talipes Equinovalgus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0265654 BXGD005559 Tarsal Coalition Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0281899 BXGD006788 Prolapsed lumbar disc Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0333068 BXGD006920 Flexion contracture Musculoskeletal Diseases
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0342282 BXGD007452 Multiple synostoses syndrome 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0343284 BXGD007613 Chondrodysplasia Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0345375 BXGD007730 Congenital hypoplasia of femur Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0349588 BXGD007933 Short stature
C0391826 BXGD008013 Lhermitte-Duclos disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0409348 BXGD008384 Flexion contracture of proximal interphalangeal joint
C0409477 BXGD008386 Ankylosis of the elbow joint Musculoskeletal Diseases
C0409952 BXGD008399 Idiopathic osteoarthritis Musculoskeletal Diseases
C0409959 BXGD008400 Osteoarthritis, Knee Musculoskeletal Diseases
C0410528 BXGD008430 Skeletal dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0410740 BXGD008449 Acquired deformity of finger Musculoskeletal Diseases
C0424621 BXGD008536 Body Fat Distribution
C0424678 BXGD008537 Lean body mass
C0424731 BXGD008542 Single transverse palmar crease Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0426421 BXGD008561 Wide nose
C0426891 BXGD008595 Broad thumbs
C0431863 BXGD008709 Carpal synostosis
C0431890 BXGD008712 Hypoplasia of thumb Musculoskeletal Diseases
C0431904 BXGD008713 Ulnar polydactyly of fingers Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0455806 BXGD008858 Infant length
C0489786 BXGD009018 Height
C0524620 BXGD009236 Metabolic Syndrome X Nutritional and Metabolic Diseases
C0524851 BXGD009246 Neurodegenerative Disorders Nervous System Diseases
C0541764 BXGD009259 Delayed bone age
C0562350 BXGD009476 Hip circumference
C0576226 BXGD009527 Short foot
C0595939 BXGD009629 Stillbirth Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0685381 BXGD009809 Congenital hypoplasia of radius Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0853087 BXGD010964 Nail abnormality Pathological Conditions, Signs and Symptoms
C0877165 BXGD011338 Short phalanx of finger
C0878659 BXGD011380 Disproportionate short stature Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0919677 BXGD011435 Protein C measurement
C1168438 BXGD011793 Protein C antigen measurement
C1261473 BXGD011855 Sarcoma Neoplasms
C1266044 BXGD011940 Collecting Duct Carcinoma of the Kidney Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1300268 BXGD012276 Brachydactyly syndrome type C Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C1306065 BXGD012352 DEVELOPMENTAL DYSPLASIA OF THE HIP 1
C1306710 BXGD012372 Facial asymmetry Pathological Conditions, Signs and Symptoms
C1328407 BXGD012465 Hip Dysplasia Musculoskeletal Diseases; Wounds and Injuries
C1336708 BXGD012852 Testicular Germ Cell Tumor Neoplasms; Male Urogenital Diseases; Endocrine System Diseases
C1384584 BXGD012943 Generalized osteoarthritis Musculoskeletal Diseases
C1518922 BXGD013229 peak expiratory flow (procedure)
C1578482 BXGD013427 Valgus deformities of feet Musculoskeletal Diseases
C1611743 BXGD013456 Familial (FPAH)
C1739384 BXGD013736 Angel shaped phalangoepiphyseal dysplasia Musculoskeletal Diseases
C1832117 BXGD013798 Short humerus
C1832119 BXGD013799 Fibular hypoplasia
C1832702 BXGD013871 BRACHYDACTYLY, TYPE A2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1832708 BXGD013872 MULTIPLE SYNOSTOSES SYNDROME 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1834034 BXGD013951 Aplasia/Hypoplasia of the middle phalanx of the 5th finger
C1834060 BXGD013954 Short middle phalanx of the 5th finger
C1836186 BXGD014089 Fibular aplasia
C1836192 BXGD014092 Aplasia/Hypoplasia involving the metacarpal bones
C1836193 BXGD014093 Synostosis of carpal bones
C1836195 BXGD014094 Short toe
C1836212 BXGD014096 Proximal/middle symphalangism of 5th finger
C1837084 BXGD014195 Short metacarpal
C1837835 BXGD014279 Bilateral talipes equinovarus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1839829 BXGD014413 Short distal phalanx of finger
C1840555 BXGD014476 Hip Dysplasia, Congenital, Nonsyndromic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1842229 BXGD014505 Broad metacarpals
C1843108 BXGD014556 Short palm
C1844709 BXGD014667 Radial deviation of the 2nd finger
C1844891 BXGD014691 Ulnar deviation of the 2nd finger
C1846950 BXGD014848 Short middle phalanx of finger
C1848673 BXGD014963 Hypoplastic feet
C1849020 BXGD014996 Short metatarsal
C1849311 BXGD015034 Short 1st metacarpal
C1849937 BXGD015091 Disproportionate short-limb short stature
C1850049 BXGD015101 Clinodactyly of the 5th finger
C1850259 BXGD015125 Short tibia
C1855340 BXGD015490 Bowing of the long bones
C1856732 BXGD015639 Aplasia/Hypoplasia of the fibula
C1856738 BXGD015640 Fibular hypoplasia and complex brachydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1856742 BXGD015641 Malaligned carpal bone
C1856746 BXGD015642 Deformed tarsal bones
C1856749 BXGD015643 Aplastic/hypoplastic toenail
C1856912 BXGD015656 Shortening of all middle phalanges of the fingers
C1857108 BXGD015677 Limitation of joint mobility
C1858430 BXGD015792 Death in infancy
C1859399 BXGD015886 Radial bowing
C1859481 BXGD015900 Abnormal finger flexion creases
C1860105 BXGD015953 Severe short-limb dwarfism
C1860107 BXGD015954 Distal femoral bowing
C1860111 BXGD015955 Abnormally shaped carpal bones
C1860179 BXGD015963 Valgus hand deformity
C1860182 BXGD015964 Aplasia/Hypoplasia of metatarsal bones
C1860614 BXGD015992 ULNAR HYPOPLASIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1860828 BXGD016005 Cone-shaped epiphyses of the middle phalanges of the hand
C1861385 BXGD016043 SYMPHALANGISM, PROXIMAL Musculoskeletal Diseases
C1862095 BXGD016100 Bilateral single transverse palmar creases
C1862103 BXGD016103 Brachydactyly type C Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1862142 BXGD016107 Short 2nd finger
C1862144 BXGD016108 Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
C1862147 BXGD016109 Medially deviated second toe
C1862151 BXGD016110 BRACHYDACTYLY, TYPE A1 (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1862158 BXGD016112 Terminal symphalangism of hands Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1864356 BXGD016223 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE Musculoskeletal Diseases
C1864365 BXGD016224 Acromesomelia
C1865037 BXGD016289 Cone-shaped epiphysis
C1865992 BXGD016359 Short hallux
C1866656 BXGD016413 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1866730 BXGD016419 Rhizomelia
C1867131 BXGD016440 Broad hallux
C1868577 BXGD016509 Patella aplasia-hypoplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1969397 BXGD016776 Short 2nd metacarpal
C2717759 BXGD017509 Degenerative Intervertebral Discs Musculoskeletal Diseases
C2745963 BXGD017571 Kashin-Beck Disease Musculoskeletal Diseases
C2751826 BXGD017744 Multiple Synostoses Syndrome 3 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C2919142 BXGD017867 Short Stature, CTCAE
C2930865 BXGD017908 Ramer Ladda syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C2930970 BXGD017921 Acromesomelic dysplasia Hunter-Thompson type Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C3179508 BXGD018554 Aplasia/Hypoplasia of the thumb Musculoskeletal Diseases
C3278509 BXGD018742 Spinal fusion
C3553754 BXGD019185 Absent toe
C3553764 BXGD019187 Joint hyperflexibility
C3554446 BXGD019213 BRACHYDACTYLY, TYPE A1, C
C3554614 BXGD019227 Ulnar deviation of the 3rd finger
C3714899 BXGD019437 SYMPHALANGISM, PROXIMAL, 1A Musculoskeletal Diseases
C3809104 BXGD019572 SYMPHALANGISM, PROXIMAL, 1B
C3840085 BXGD019794 Disorder of Achilles tendon
C4021390 BXGD020622 Symphalangism affecting the phalanges of the hand
C4021399 BXGD020628 Finger symphalangism
C4021427 BXGD020630 Complete duplication of distal phalanx of the thumb
C4021432 BXGD020633 Triangular shaped proximal phalanx of the 2nd finger
C4021435 BXGD020634 Short middle phalanx of the 2nd finger
C4021454 BXGD020636 Triangular epiphysis of the proximal phalanx of the 2nd finger
C4021455 BXGD020637 Enlarged epiphysis of the proximal phalanx of the 2nd finger
C4021465 BXGD020638 Pseudoepiphyses of the 2nd finger
C4021469 BXGD020639 Short 3rd finger
C4021474 BXGD020640 Short middle phalanx of the 3rd finger
C4021480 BXGD020641 Pseudoepiphyses of the 3rd finger
C4021487 BXGD020642 Triangular epiphysis of the proximal phalanx of the 3rd finger
C4021488 BXGD020643 Enlarged epiphysis of the proximal phalanx of the 3rd finger
C4021490 BXGD020644 Triangular epiphysis of the middle phalanx of the 3rd finger
C4021497 BXGD020645 Short middle phalanx of the 4th finger
C4021611 BXGD020697 Abnormality of epiphysis morphology
C4021735 BXGD020743 Abnormality of the hip bone
C4022107 BXGD020880 Aplasia of the middle phalanges of the toes
C4023122 BXGD021117 Hypersegmentation of proximal phalanx of third finger
C4023124 BXGD021118 Short digit
C4024098 BXGD021288 Aplasia/Hypoplasia of the 1st metacarpal
C4024235 BXGD021314 Stippling of the epiphysis of the distal phalanx of the thumb
C4024283 BXGD021316 Triangular shaped middle phalanx of the 2nd finger
C4024310 BXGD021318 Triangular epiphysis of the middle phalanx of the 2nd finger
C4024317 BXGD021319 Enlarged epiphysis of the middle phalanx of the 2nd finger
C4024349 BXGD021322 Triangular shaped proximal phalanx of the 3rd finger
C4024362 BXGD021323 Triangular shaped middle phalanx of the 3rd finger
C4024441 BXGD021324 Enlarged epiphysis of the middle phalanx of the 3rd finger
C4024552 BXGD021327 Triangular shaped middle phalanx of the 5th finger
C4025080 BXGD021547 Hypersegmentation of proximal phalanx of second finger
C4025089 BXGD021552 Shortening of all proximal phalanges of the fingers
C4025093 BXGD021554 Cuboidal metacarpal
C4025117 BXGD021560 Metacarpophalangeal synostosis
C4025660 BXGD021715 Abnormality of the ankles
C4025662 BXGD021716 Abnormality of the ulna
C4025663 BXGD021717 Abnormality of tibia morphology
C4025675 BXGD021726 Abnormality of the radius
C4049938 BXGD021956 Physical Activity Measurement
C4082144 BXGD022081 Metatarsal Valgus Musculoskeletal Diseases
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4551564 BXGD023352 Narrow nasal bridge
C4551570 BXGD023357 2-3 toe syndactyly
C4551649 BXGD023382 Congenital Dysplasia Of The Hip Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C4551826 BXGD023414 Symphalangism-brachydactyly syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C4552513 BXGD023513 Temporomandibular joint osteoarthritis
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000436 Glycerol 92.09
BXGC0003705 Chloride 35.45
BXGC0004266 2-Propanol 60.1
BXGC0006198 Citric acid 192.12
BXGC0037687 (4S)-2-methylpentane-2,4-diol 118.1
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein