Autoimmune Disease, Multisystem, With Facial Dysmorphism; Admfd
Genes related to Autoimmune Disease, Multisystem, With Facial Dysmorphism; Admfd
- ITCH
Clinical Features
Top most frequent phenotypes and symptoms related to Autoimmune Disease, Multisystem, With Facial Dysmorphism; Admfd
- Global developmental delay
- Generalized hypotonia
- Pica
- Failure to thrive
- Ptosis
- Abnormal facial shape
- Low-set ears
- Hepatomegaly
- Macrocephaly
- Frontal bossing
Click here to know more about Mendelian.
Incidence and onset information
— Not enough data available about incidence and published cases.
Accelerate your rare disease diagnosis with us
Learn more
Autoimmune Disease, Multisystem, With Facial Dysmorphism; Admfd Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
ALPS/autoimmunity panel.
By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.
CASP8, AIRE, KRAS, NRAS, FOXP3, FAS, FASLG, CASP10, LRBA, FADD, IL2RA, ITCH
Specificity
9 %
Genes
100 % |
Immune dysregulation Panel.
By CeGaT GmbH in Germany.
CASP8, AP3B1, AIRE, PRF1, TREX1, FOXP3, LYST, SH2D1A, RAB27A, UNC13D, FAS, STX11, XIAP, FASLG, CASP10, STXBP2, PRKCD, CARD11, IL2RA, ITCH , (...)
View the complete list with 2 more genes
Specificity
5 %
Genes
100 % |
Invitae Monogenic Autoimmunity Panel.
By Invitae in United States.
STAT1, CASP8, AP3B1, UNG, CYBA, STAT3, PNP, AIRE, RMRP, PRF1, CYBB, SLC7A7, WAS, BTK, SAMHD1, RNASEH2A, RNASEH2C, RNASEH2B, TREX1, TBX1 , (...)
View the complete list with 53 more genes
Specificity
2 %
Genes
100 % |
Invitae Primary Immunodeficiency Panel.
By Invitae in United States.
PMS2, STAT1, SLC37A4, CASP8, TLR3, HAX1, AP3B1, UNG, TAP1, TAZ, TCN2, AK2, SLC35C1, CYBA, STAT3, ADA, MOGS, IL2RG, PNP, AIRE , (...)
View the complete list with 187 more genes
Specificity
1 %
Genes
100 % |
ITCH.
By Fulgent Genetics Fulgent Genetics in United States.
ITCH
Specificity
100 %
Genes
100 % |
CEN4GEN Breast cancer: Extended gene sequencing Panel.
By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.
BRCA1, BRCA2, PTEN, TP53, RB1, RET, SEPT9, FGFR2, ATM, CDH1, CDKN2A, FGFR1, GATA3, NEK2, ERBB3, EP300, BAP1, PIK3CA, EGFR, AKT1 , (...)
View the complete list with 25 more genes
Specificity
3 %
Genes
100 % |
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like RIBOFLAVIN DEFICIENCY; RBFVD POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT; PHARC LIGNEOUS CONJUNCTIVITIS AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK FLOATING-HARBOR SYNDROME; FLHS JOUBERT SYNDROME 14; JBTS14