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Term:
autosomal recessive cutis laxa type IC (DOID:0070139)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
actinobacillosis 
actinomycosis +  
articular cartilage disease +   
asphyxia neonatorum +   
autosomal recessive cutis laxa type IA  
autosomal recessive cutis laxa type IB  
autosomal recessive cutis laxa type IC  
A autosomal recessive cutis laxa type I that has_material_basis_in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13. (DO)
bacteriuria 
bladder disease +   
bronchial disease +   
CAKUT +   
cartilage cancer 
Ciliary Motility Disorders +   
diarrhea +   
discitis 
esophageal disease +   
Fibrocartilaginous Embolism 
gastroenteritis +   
gastrointestinal anthrax +  
Gastrointestinal Hemorrhage +   
Gastrointestinal Motility Disorders +   
Gastrointestinal Neoplasms +   
gastrointestinal tuberculosis +  
gastrointestinal tularemia 
influenza +   
INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD  
intestinal disease +   
Keutel Syndrome  
kidney disease +   
Kilquist Syndrome  
Laryngomalacia +   
lower respiratory tract disease +   
lung disease +   
NATURAL KILLER CELL ENTEROPATHY  
neonatal urinary tract infectious disease 
Osteochondritis +   
Pectus Carinatum  
Phospholipase A2, Group IVA, Deficiency of  
pleural disease +   
pyuria 
Respiration Disorders +   
respiratory allergy +   
Respiratory System Abnormalities +   
Respiratory Tract Fistula +   
Respiratory Tract Granuloma +   
Respiratory Tract Infections +   
Respiratory Tract Neoplasms +   
Siegler Brewer Carey Syndrome 
stomach disease +   
thoracic disease +   
Tietze's syndrome  
tracheal disease +   
Tracheobronchomalacia +   
upper respiratory tract disease +   
ureteral disease +   
urethral disease +   
urinary system benign neoplasm +   
urinary system cancer +   
urinary tract infection +   
urinary tract obstruction +   
Urination Disorders +   
urofacial syndrome +   
urolithiasis +   
Visceral Prolapse 

Synonyms
Exact Synonyms: ARCL1C ;   URDS ;   Urban-Rifkin-Davis syndrome ;   autosomal recessive cutis laxa type 1C ;   cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities
Primary IDs: MESH:C567716
Alternate IDs: OMIM:613177
Xrefs: ORDO:221145
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/19836010 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.