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Neonatal Progeroid Syndrome (DOID:9008367)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
progeria +     
Acrogeria, Gottron Type 
Bird Headed Dwarfism Montreal Type 
Bowen-Conradi syndrome  
Camptodactyly Syndrome Guadalajara Type 2 
Cartwright Nelson Fryns Syndrome 
Craniomicromelic Syndrome 
fetal akinesia deformation sequence syndrome +   
Fetal Akinesia Syndrome, X-Linked 
GRACILE syndrome  
Granddad Syndrome 
Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence 
Hoyeraal Hreidarsson Syndrome  
IMAGe syndrome  
IMAGEI Syndrome  
Lambotte Syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Microcephalic Osteodysplastic Primordial Dwarfism +   
Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects 
Neonatal Progeroid Syndrome  
Neonatal Progeroid syndrome or Wiedemann-Rautenstrauch syndrome (WDRTS) is a rare autosomal recessive neonatal progeroid disorder characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment. Average survival in WDRTS is 7 months, although survival into the third decade of life has been reported. WDRTS is caused by compound heterozygous mutation in the POLR3A gene on chromosome 10q22. (OMIM)
Neu-Laxova syndrome 1  
Penttinen-Aula Syndrome  
Permanent Neonatal Diabetes Mellitus, with Cerebellar Agenesis  
Petty Laxova Wiedemann Syndrome 
Premature Aging Syndrome, Okamoto Type 
Progeria Short Stature Pigmented Nevi 
Progeria Syndrome, Childhood-Onset +   
Progeroid Facial Appearance with Hand Anomalies 
Progeroid Syndrome, Congenital, Petty Type  
Ray Peterson Scott Syndrome 
Ruijs-Aalfs syndrome  
Ruvalcaba Churesigaew Myhre Syndrome 
Seckel syndrome 4  
Sharma Kapoor Ramji Syndrome 
Short Stature and Locking Fingers 
Silver-Russell Syndrome 3  
Thymic-Renal-Anal-Lung Dysplasia 
trichohepatoenteric syndrome +   
Woods Leversha Rogers Syndrome 

Exact Synonyms: WDRTS ;   Wiedemann-Rautenstrauch syndrome ;   neonatal pseudo-hydrocephalic progeroid syndrome
Primary IDs: MESH:C536423
Alternate IDs: OMIM:264090
Xrefs: NCI:C121565

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