Phenotypes for disease #05608 (SCID (immunodeficiency, severe combined (SCID)))

40 entries on 1 page. Showing entries 1 - 40.
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0000179415 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239198
0000179416 severe combined immunodeficiency - see paper; ..., T- B+ SCID Familial, autosomal recessive - - - - Johan den Dunnen 00239199
0000179417 severe combined immunodeficiency - see papr; ..., T- B+ SCID Familial, autosomal recessive - - - - Johan den Dunnen 00239200
0000179418 severe combined immunodeficiency - see paper; ..., T- B+ NK- SCID Familial, autosomal recessive - - - - Johan den Dunnen 00239201
0000179419 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239202
0000179420 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239203
0000179421 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239205
0000179422 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239230
0000179423 severe combined immunodeficiency - see paper; ... Unknown - - - - Johan den Dunnen 00239231
0000179424 severe combined immunodeficiency - see paper; ... Unknown - - - - Johan den Dunnen 00239233
0000179425 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239234
0000179426 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239232
0000179427 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239212
0000179428 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239219
0000179429 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239218
0000179430 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239216
0000179431 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239217
0000179432 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239214
0000179433 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239213
0000179434 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239215
0000179435 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239239
0000179436 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239224
0000179437 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239226
0000179438 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239227
0000179439 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239225
0000179440 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239235
0000179441 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239237
0000179442 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239223
0000179443 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239207
0000179444 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239209
0000179445 severe combined immunodeficiency - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00239210
0000268612 T-B-NK+ SCID - - Familial, autosomal recessive - - - - Marieke De Bruyne 00373334
0000306411 severe combined immunodeficiency IMD73B see paper; ..., temperature instability, hyperbilirubinemia, agranulocytosis, severe lymphopenia without associated anemia or thrombocytopenia Isolated (sporadic) - - - - Johan den Dunnen 00414615
0000325665 SCID - Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Familial, autosomal recessive - - - - Rabab Elhawary 00435477
0000338866 SCID-Omenn syndrome - see paper; ..., failure to thrive; diarrhea; <7d-skin rash; recurrent infections; no systemic inflammation; no hepatomegaly; lymphadenopathy; alopecia; dysmorphic (overfolded helices, hypoplasia alea nasi, cone-shaped teeth, hypodontia); 12w-hematopoietic stem cell transplantation Isolated (sporadic) 18y - - - Johan den Dunnen 00449695
0000338867 SCID-Omenn syndrome - see paper; ..., 2y-deceased; failure to thrive; diarrhea; 14d-skin rash; recurrent infections; systemic inflammation; no hepatomegaly; no lymphadenopathy; alopecia; mild dysmorphic facial features (protruding ears, pointed chin), adducted left thumb, hypospadias, micropenis, dysplastic nails; 130w-hematopoietic stem cell transplantation Isolated (sporadic) 2y - - - Johan den Dunnen 00449696
0000338868 SCID-Omenn syndrome - see paper; ..., 16y-deceased; failure to thrive; diarrhea; 21d-skin rash; recurrent infections; no systemic inflammation; hepatomegaly; no lymphadenopathy; alopecia; no dysmorphism; 11w-hematopoietic stem cell transplantation Isolated (sporadic) 6y - - - Johan den Dunnen 00449697
0000338869 SCID-Omenn syndrome - see paper; ..., 11w-deceased; failure to thrive; diarrhea; 7d-skin rash; recurrent infections; no systemic inflammation; hepatomegaly; no lymphadenopathy; alopecia; no dysmorphism; 16w-hematopoietic stem cell transplantation Isolated (sporadic) 13y - - - Johan den Dunnen 00449698
0000338870 SCID-Omenn syndrome - see paper; ..., 4y-deceased; failure to thrive; diarrhea; 56d-skin rash; recurrent infections; no systemic inflammation; no hepatomegaly; lymphadenopathy; no dysmorphism; 12w-hematopoietic stem cell transplantation Isolated (sporadic) 4y - - - Johan den Dunnen 00449699
0000338871 SCID-Omenn syndrome - see paper; ..., no failure to thrive; diarrhea; <7d-skin rash; no recurrent infections; no systemic inflammation; no hepatomegaly; no lymphadenopathy; no alopecia; no dysmorphism; 9w-hematopoietic stem cell transplantation Isolated (sporadic) 1y - - - Johan den Dunnen 00449700
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