syndromic multisystem autoimmune disease due to ICTH deficiency
human disease
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syndromic multisystem autoimmune disease due to ICTH deficiency
Summary
syndromic multisystem autoimmune disease due to ICTH deficiency is a developmental defect during embryogenesis[1].
Key Facts
- syndromic multisystem autoimmune disease due to ICTH deficiency's instance of is recorded as developmental defect during embryogenesis[2].
- syndromic multisystem autoimmune disease due to ICTH deficiency's instance of is recorded as rare disease[3].
- syndromic multisystem autoimmune disease due to ICTH deficiency's instance of is recorded as class of disease[4].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[5].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of lung disease[6].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of immunodeficiency syndrome with autoimmunity[7].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of autoimmune connective tissue disorder[8].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of genetic syndromic intellectual disability[9].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of rare genetic intestinal disease[10].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of intractable diarrhea of infancy[11].
- syndromic multisystem autoimmune disease due to ICTH deficiency is a type of rare genetic respiratory disease[12].
- syndromic multisystem autoimmune disease due to ICTH deficiency's genetic association is recorded as ITCH[13].
- syndromic multisystem autoimmune disease due to ICTH deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_228426[14].