Phenotypes for disease #05375 (progeroid (progeroid syndrome (premature aging)))

7 entries on 1 page. Showing entries 1 - 7.
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0000122525 - - see paper; ..., affected by a segmental progeroid syndrome Familial, autosomal recessive - - - - Davor Lessel 00150130
0000185025 - - progeroid syndrome, neonatal (Wiedemann-Rautenstrauch syndrome) Familial, autosomal recessive - - - - Philippe Campeau 00245067
0000232020 progeroid syndrome XFEPS see paper; ..., frequent sunburns, unique combination of progeroid symptoms, neurologic; hepatobiliary, musculoskeletal and haematopoietic symptoms Familial, autosomal recessive 15y - - - Johan den Dunnen 00306176
0000232021 progeroid syndrome XFEPS see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00132618
0000232022 progeroid syndrome - see paper; ..., 54y-bilateral cataracts , tight atrophic skin: 30y-graying and thinning of hair; type II diabetes mellitus, osteoporosis, overall aged appearance; 68y-height 162 cm, weight 40 kg; 56y-papillary thyroid cancer; no cognitive impairment, no sun sensitivity; sister possibly affected Unknown - - - - Johan den Dunnen 00132619
0000257153 progeroid syndrome - see paper; ..., triangular face, prominent eyes, crooked nose, septum deviation, mandibular hypoplasia; no juvenile alopezia, no loss of eyebrows, thin skin, prominent veins, no cutis laxa, no patchy hyperpigmentation, no dystrophic nails; generalized lipoatrophy; microcephaly; Wormian bones, no open cranial sutures, dental crowding, supernumerary teeth, delayed dentition; short stature, low bone density, hypoplastic clavicles, no osteolytic foci, no joint hyperlaxity, no limited joint mobility; intra-uterine growth retardation; no atherosclerosis; intention tremor; no developmental delay Isolated (sporadic) - - - - Johan den Dunnen 00222778
0000257154 progeroid syndrome - see paper; ..., triangular face, prominent eyes, crooked nose, septum deviation, mandibular hypoplasia; no juvenile alopezia, no loss of eyebrows, thin skin, prominent veins, no cutis laxa, no patchy hyperpigmentation, no dystrophic nails; generalized lipoatrophy; microcephaly; Wormian bones, no open cranial sutures, dental crowding, supernumerary teeth, delayed dentition; no short stature (32th percentile, growth hormone treatment), no low bone density, hypoplastic clavicles, no osteolytic foci, no joint hyperlaxity, no limited joint mobility; no intra-uterine growth retardation; no atherosclerosis; intention tremor; no developmental delay Isolated (sporadic) - - - - Johan den Dunnen 00222781
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