Disease association ontology term - MONDO:0015333 - progeroid syndrome
Term summary
ID
MONDO:0015333
Name
progeroid syndrome
Ontology or CV name
Disease association
Definition
A group of rare genetic disorders which mimic physiological aging, making affected individuals appear to be older than they are.
Parents
is_a
hereditary disease
is_a
premature aging syndrome
is_a
developmental defect during embryogenesis
Annotation
Disease association
MONDO:0700300
-
achalasia-progeroid syndrome
References:
PB_REF:0000006
Genes:
cwf26 (SPCC1620.10)
MONDO:0016006
-
Cockayne syndrome
References:
PB_REF:0000003
Genes:
ckn1 (SPBC577.09)
rhp26 (SPCP25A2.02c)
MONDO:0019569
-
Cockayne syndrome type 1
References:
PB_REF:0000006
Genes:
ckn1 (SPBC577.09)
MONDO:0019570
-
Cockayne syndrome type 2
References:
PB_REF:0000006
Genes:
rhp26 (SPCP25A2.02c)
MONDO:0700301
-
Fischer-Zirnsak progeroid syndrome
References:
PB_REF:0000006
Genes:
spt7 (SPBC25H2.11c)
MONDO:0012853
-
Fontaine progeroid syndrome
References:
PB_REF:0000006
Genes:
SPBC12D12.05c
MONDO:0014157
-
mandibular hypoplasia-deafness-progeroid syndrome
References:
PB_REF:0000006
Genes:
cdc6 (SPBC336.04)
MONDO:0030880
-
mandibuloacral dysplasia progeroid syndrome
References:
PB_REF:0000006
Genes:
mtx2 (SPAC589.04)
MONDO:0859147
-
Marbach-Rustad progeroid syndrome
References:
PB_REF:0000006
Genes:
lem2 (SPAC18G6.10)
MONDO:0010196
-
Werner syndrome
References:
PB_REF:0000006
PMID:10497270
Genes:
rqh1 (SPAC2G11.12)
MONDO:0009910
-
Wiedemann-Rautenstrauch syndrome
References:
PB_REF:0000006
Genes:
rpc1 (SPBC651.08c)
MONDO:0012590
-
XFE progeroid syndrome
References:
PB_REF:0000006
Genes:
rad16 (SPCC970.01)
