Phenotypes for disease #01528 (PSACH (pseudoachondroplasia (PSACH)), OMIM:177170)

40 entries on 1 page. Showing entries 1 - 40.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000186998 moderately severe - - Unknown - - - - - Michael Briggs 00247806
0000187001 mild - - Unknown - - - - - LOVD 00247836
0000187003 mild - - Unknown - - - - - LOVD 00247838
0000187004 severe - - Isolated (sporadic) - - - - - LOVD 00247839
0000187005 severe - - Isolated (sporadic) - - - - - LOVD 00247840
0000187006 severe - - Isolated (sporadic) - - - - - LOVD 00247841
0000187007 mild - - Unknown - - - - - LOVD 00247842
0000187008 severe - - Unknown - - - - - LOVD 00247843
0000187009 mild - - Unknown - - - - - LOVD 00247844
0000187010 mild - - Unknown - - - - - LOVD 00247845
0000187011 severe - - Isolated (sporadic) - - - - - LOVD 00247846
0000187012 severe - - Unknown - - - - - LOVD 00247860
0000187013 mild - - Isolated (sporadic) - - - - - LOVD 00247863
0000187016 mild - - Isolated (sporadic) - - - - - LOVD 00247866
0000187018 severe - - Isolated (sporadic) - - - - - LOVD 00247868
0000187019 severe - - Isolated (sporadic) - - - - - LOVD 00247869
0000187020 mild - - Familial - - - - - LOVD 00247870
0000187022 mild - - Isolated (sporadic) - - - - - LOVD 00247872
0000187023 severe - - Isolated (sporadic) - - - - - LOVD 00247873
0000187027 moderately severe - - Familial - - - - - Michael Briggs 00247922
0000187037 - - - Familial - - - - - LOVD 00247882
0000187038 - - - Familial - - - - - Michael Briggs 00247925
0000187039 - - - Familial - - - - - Michael Briggs 00247927
0000187040 - - - Familial - - - - - Michael Briggs 00247932
0000187041 - - - Familial - - - - - Michael Briggs 00247949
0000187042 - - - Familial - - - - - Michael Briggs 00247968
0000187045 - - - Familial - - - - - Michael Briggs 00247986
0000187047 - - - Familial - - - - - LOVD 00247798
0000187049 - - - Familial - - - - - Michael Briggs 00247821
0000187055 - - - Isolated (sporadic) - - - - - LOVD 00247799
0000187056 - - - Isolated (sporadic) - - - - - LOVD 00247800
0000187057 - - - Isolated (sporadic) - - - - - LOVD 00247834
0000274666 Short stature; abnormal bones (Skeletal) - Pseudoachondroplasia Familial - - - - - LOVD 00380813
0000307887 - - - Isolated (sporadic) - - - - - Kosei Hasegawa 00416121
0000307890 - - - Isolated (sporadic) - - - - - Kosei Hasegawa 00416124
0000307891 - - - Isolated (sporadic) - - - - - Kosei Hasegawa 00416125
0000307892 - - - Isolated (sporadic) - - - - - Kosei Hasegawa 00416126
0000307893 - - - Isolated (sporadic) - - - - - Kosei Hasegawa 00416127
0000309867 no hypotonia; normal developmental milestones; normal groth/feeding; height 121 cm (-2.5 SD); rhizomelic shortening upper and lower extremities; OFC 56cm; no kyphosis; short, broad fingers; no acromelia; short broad toes; broad nasal bridge, thick eyebrows, synophrys, prominent chin; no cranial anomalies; normal palate; platyspondyly; metaphyseal changes; short metacarp and metatarsal, disostosis peripheral; 9y-no delayed bone age; constipation, umbilical hernia in the past (now normal), hypertrichosis pseudoachondroplasia - Familial, autosomal recessive 10y - 3y short stature, dysmorphism - Johan den Dunnen 00418531
0000338928 - - - Familial, autosomal dominant - - - - - Dan Feng Fang 00449783
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