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Ontology Browser
Term:
Familial Synovial Chondromatosis with Dwarfism (DOID:9003213)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
Dwarfism +     
Synovial Chondromatosis +    
3-M syndrome +   
Aarskog syndrome +   
Abuse Dwarfism Syndrome 
achondroplasia +   
acromesomelic dysplasia +   
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
Alopecia Contractures Dwarfism Mental Retardation 
AMED syndrome  
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
anauxetic dysplasia +   
Astley-Kendall Syndrome 
Asymmetric Short Stature Syndrome 
Atelosteogenesis Type 3  
Bangstad Syndrome 
Bird Headed Dwarfism Montreal Type 
Boomerang dysplasia  
Brachydactylous Dwarfism Mseleni Type 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brunoni Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
Cantu Sanchez-Corona Fragoso Syndrome 
Chondrodysplasia Calcificans Metaphysealis 
Cockayne syndrome +   
congenital hypothyroidism +   
De Sanctis-Cacchione syndrome  
Desbuquois dysplasia +   
Diabetes, Deafness, Developmental Delay, and Short Stature Syndrome  
diastrophic dysplasia +   
diphthamide deficiency syndrome +   
Disproportionate Short Stature with Ptosis and Valvular Heart Lesions 
Dwarfism Stiff Joint Ocular Abnormalities 
Dwarfism with Tall Vertebrae 
Dwarfism, Levi Type 
Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone 
Dyggve-Melchior-Clausen disease +   
Dyssegmental Dysplasia with Glaucoma 
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Familial Dwarfism with Muscle Spasms 
Familial Synovial Chondromatosis with Dwarfism 
fibrochondrogenesis +   
GARG-MISHRA PROGEROID SYNDROME  
geroderma osteodysplasticum  
Growth Hormone Insensitivity with Immune Dysregulation +   
Growth Retardation, Developmental Delay, Coarse Facies, and Early Death  
Hadziselimovic Syndrome 
hypochondroplasia  
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
intellectual developmental disorder with abnormal behavior, microcephaly, and short stature  
intellectual developmental disorder with short stature and behavioral abnormalities  
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS  
isolated growth hormone deficiency +   
JOINT LAXITY, SHORT STATURE, AND MYOPIA  
Juberg Hayward Syndrome  
Kenny-Caffey syndrome type 2  
Keratosis Follicularis, Dwarfism, and Cerebral Atrophy 
Kniest dysplasia  
Laplane Fontaine Lagardere Syndrome 
Laron syndrome  
Lessel-Kubisch Syndrome  
Mental Retardation, Macrocephaly, Short Stature and Craniofacial Dysmorphism 
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type 
Mesomelic Dwarfism Reinhardt Pfeiffer Type 
Metatropic Dwarfism, Type II 
metatropic dysplasia  
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microcephalic Primordial Dwarfism Toriello Type 
Microcephaly, Short Stature, and Impaired Glucose Metabolism +   
Microcephaly, Short Stature, and Polymicrogyria with or without Seizures  
Mollica Pavone Antener Syndrome 
Mosaic Variegated Aneuploidy Syndrome 6  
mulibrey nanism  
Nievergelt Syndrome 
Oculopalatocerebral Syndrome 
Oliver-McFarlane syndrome  
otospondylomegaepiphyseal dysplasia, autosomal recessive  
parastremmatic dwarfism  
PRIMORDIAL DWARFISM-IMMUNODEFICIENCY-LIPODYSTROPHY SYNDROME  
Proportionate Dwarfism with Hip Dislocation 
Pseudodiastrophic Dysplasia 
rapadilino syndrome  
Robinow syndrome +   
Rommen Mueller Sybert Syndrome 
Ruvalcaba Syndrome 
Seckel Like Syndrome Type Buebel 
Seckel syndrome 1  
Seckel syndrome 2  
Seckel Syndrome 3 
Seckel syndrome 4  
Short Limb Dwarfism Al Gazali Type  
Short Stature and Facioauriculothoracic Malformations 
Short Stature and Microcephaly with Genital Anomalies  
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES  
Short Stature with Nonspecific Skeletal Abnormalities  
SHORT STATURE, DAUBER-ARGENTE TYPE  
Short Stature, Developmental Delay, and Congenital Heart Defects  
Short Stature, Facial Dysmorphism, and Skeletal Anomalies with or without Cardiac Anomalies +   
short stature, hearing loss, retinitis pigmentosa, and distinctive facies  
Short Stature, Impaired Intellectual Development, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, and Atypical Clefting 
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION  
SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY  
SHORT STATURE-MICROGNATHIA SYNDROME  
Short Stature-Obesity Syndrome 
Silver-Russell syndrome +   
Silverman-Handmaker type dyssegmental dysplasia  
Singh Chhaparwal Dhanda Syndrome 
SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE  
Spondyloepiphyseal Dysplasia Tarda, Toledo Type 
spondylometaepiphyseal dysplasia, short limb-hand type  
spondylometaphyseal dysplasia Megarbane-Dagher-Melike type  
Tessadori-van Haaften Neurodevelopmental Syndrome 1  
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Tryptophanuria with Dwarfism 
Watson syndrome  
Weill-Marchesani syndrome +   
Zaki syndrome  

Synonyms
Primary IDs: MESH:C566087
Alternate IDs: OMIM:186575

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