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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
abdominal wall malformation +  
acrogeria 
acroosteolysis-keloid-like lesions-premature aging syndrome 
angioosteohypertrophic syndrome 
ankyloblepharon filiforme-imperforate anus syndrome 
anotia 
Becker nevus syndrome +  
blindness - scoliosis - arachnodactyly syndrome 
bone fragility with contractures, arterial rupture, and deafness 
central nervous system malformation +  
cleft palate +  
congenital anomaly of kidney and urinary tract +  
congenital limb malformation +   
cutis laxa +  
cutis laxa - Marfanoid syndrome 
cysts and fistulae of the face and oral cavity +  
de Barsy syndrome +  
Desbuquois dysplasia +  
developmental anomaly of metabolic origin +  
developmental defect of the eye +   
digestive tract malformation +  
disorder of sexual differentiation +  
Ehlers-Danlos syndrome +  
facial cleft +  
Flynn-Aird syndrome 
focal dermal hypoplasia 
Hallermann-Streiff syndrome 
hemihyperplasia-multiple lipomatosis syndrome 
hereditary hemorrhagic telangiectasia +  
hereditary neurocutaneous angioma 
hydrops fetalis +  
infectious embryofetopathy +  
joint laxity, short stature, and myopia 
Larsen syndrome 
Legius syndrome 
lethal Larsen-like syndrome 
linear nevus sebaceous syndrome 
LMNA-related cardiocutaneous progeria syndrome 
macroglossia +  
Maffucci syndrome 
mandibular hypoplasia-deafness-progeroid syndrome 
marfanoid habitus-inguinal hernia-advanced bone age syndrome 
microtia 
multiple congenital anomalies/dysmorphic syndrome +   
neurofibromatosis type 1 +  
neurofibromatosis-Noonan syndrome +  
nevoid basal cell carcinoma syndrome 
phakomatosis pigmentokeratotica 
phakomatosis pigmentovascularis +  
progeroid syndrome +  
A group of rare genetic disorders which mimic physiological aging, making affected individuals appear to be older than they are.
Progeroid syndrome, Petty type 
pseudodiastrophic dysplasia 
PTEN hamartoma tumor syndrome +  
schwannomatosis 
telomere syndrome +   
toxic or drug-related embryofetopathy +  
TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations +  
urogenital tract malformation +   

Synonyms
Exact Synonyms: DOID:0081332 ;   Orphanet:139033
Alternate IDs: MONDO:0015333
Xrefs: DOID:0081332 ;   GARD:19906 ;   NANDO:2100221 ;   ORDO:139033
Definition Sources: Wikipedia:Progeroid_syndromes

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