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Term:
Fanconi-like syndrome (DOID:0090066)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2)
Parent Terms Term With Siblings Child Terms
Abdominal Chemodectomas with Cutaneous Angiolipomas 
acanthoma +  
agammaglobulinemia +   
allergic contact dermatitis +   
Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis, and Lymphedema  
Antibody Deficiency due to Defect in CD19 
ataxia telangiectasia +   
Autoinflammation, Antibody Deficiency, and Immune Dysregulation, PLCG2-Associated  
B cell deficiency +   
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
Banti's Syndrome  
Bazex-Dupre-Christol Syndrome 
Becker Nevus Syndrome 
Blue Rubber Bleb Nevus Syndrome  
Brooke-Spiegler syndrome  
C1q Deficiency  
C9 Deficiency with Dermatomyositis 
Calcifying Epithelial Odontogenic Tumor 
CARD11 Immunodeficiency  
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cartilage Hair Hypoplasia Like Syndrome 
cartilage-hair hypoplasia  
Cd4+ Lymphocyte Deficiency  
CD8 Deficiency, Familial  
COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA  
Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia  
Combined Inflammatory and Immunologic Defect 
combined T cell and B cell immunodeficiency +   
common variable immunodeficiency +   
complement component 9 deficiency  
complement deficiency +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Davenport Donlan Syndrome 
Deltaretrovirus Infections +   
Dermatopathia Pigmentosa Reticularis  
DNA ligase IV deficiency  
Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency, Autosomal Dominant  
Endotoxin Hyporesponsiveness  
Enteropathy, Familial, with Villous Edema and Immunoglobulin G2 Deficiency 
EVANS SYNDROME, IMMUNODEFICIENCY, AND PREMATURE IMMUNOSENESCENCE ASSOCIATED WITH TRIPEPTIDYL-PEPTIDASE II DEFICIENCY  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
familial cold autoinflammatory syndrome +   
Familial Cutaneous Collagenoma  
Familial Cutaneous Papillomatosis 
Familial Multiple Trichodiscomas 
Fanconi-like syndrome  
A syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies. (DO)
Giant Pigmented Hairy Nevus  
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency 
Griscelli syndrome +   
Hamartoma, Precalcaneal Congenital Fibrolipomatous 
Hepatic Venoocclusive Disease with Immunodeficiency  
Hereditary Leiomyomatosis and Renal Cell Cancer  
human immunodeficiency virus infectious disease +   
Hypoglobulinemia and Absent B Cells 
IL21R Immunodeficiency  
Immune Deficiency Disease  
Immune Deficiency, Familial Variable 
IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS  
Immunodeficiency 12  
Immunodeficiency 14  
IMMUNODEFICIENCY 15A  
Immunodeficiency 15B  
Immunodeficiency 16  
Immunodeficiency 19  
Immunodeficiency 20  
Immunodeficiency 21  
Immunodeficiency 22  
Immunodeficiency 23  
IMMUNODEFICIENCY 24  
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES  
Immunodeficiency 27B  
IMMUNODEFICIENCY 28  
IMMUNODEFICIENCY 29  
Immunodeficiency 30  
Immunodeficiency 31A  
IMMUNODEFICIENCY 31B  
IMMUNODEFICIENCY 31C  
Immunodeficiency 32A  
Immunodeficiency 32B  
Immunodeficiency 36  
Immunodeficiency 37  
Immunodeficiency 38, with Basal Ganglia Calcification  
Immunodeficiency 39  
Immunodeficiency 40  
Immunodeficiency 42  
Immunodeficiency 44  
Immunodeficiency 45  
Immunodeficiency 46  
Immunodeficiency 47  
Immunodeficiency 48  
Immunodeficiency 49  
Immunodeficiency 50  
Immunodeficiency 51  
Immunodeficiency 52  
Immunodeficiency 53  
Immunodeficiency 55  
IMMUNODEFICIENCY 58  
Immunodeficiency due to Defect in CD3-Epsilon  
Immunodeficiency due to Defect in CD3-Gamma  
Immunodeficiency due to Defect in CD3-Zeta  
Immunodeficiency due to Defect in MAPBP-Interacting Protein  
Immunodeficiency due to Ficolin 3 Deficiency  
Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist 
Immunodeficiency without Anhidrotic Ectodermal Dysplasia  
IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA  
Immunodeficiency, Gonadal Dysgenesis, and Pulmonary Fibrosis 
Immunodeficiency, Partial Combined, with Absence of HLA Determinants and Beta-2-Microglobulin from Lymphocytes 
immunodeficiency-centromeric instability-facial anomalies syndrome +   
immunoglobulin beta deficiency 
IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY  
Inosine Phosphorylase Deficiency, Immune Defect Due To 
INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES  
Interleukin 2 Receptor, Alpha, Deficiency of  
Invasive Pneumococcal Disease, Recurrent Isolated, 1  
Invasive Pneumococcal Disease, Recurrent Isolated, 2  
IRAK4 Deficiency  
Kotzot-Richter Syndrome 
leukocyte adhesion deficiency +   
Lichtenstein Syndrome 
LUNG DAMAGE, IMMUNODEFICIENCY AND CHROMOSOME BREAKAGE SYNDROME  
Lymphoblastic Transformation, Intrinsic Defect in 
Lymphoid System Deterioration, Progressive 
Lymphokine Deficiency 
lymphopenia +   
Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis 
lymphoproliferative syndrome +   
MASP2 Deficiency  
MYD88 Deficiency  
Myelocerebellar Disorder  
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
Natural Killer Cell and Glucocorticoid Deficiency with DNA Repair Defect  
NEMO Mutation with Immunodeficiency 
neurilemmomatosis  
Neutrophil Immunodeficiency Syndrome  
Nezelof syndrome 
PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING  
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal  
Pancytopenia and Occlusive Vascular Disease 
Phacomatosis Pigmentokeratotica 
phagocyte bactericidal dysfunction +   
Progressive Mucinous Histiocytosis 
Properdin Deficiency, Type II  
Properdin Deficiency, Type III  
Reactive Angioendotheliomatosis 
Riddle syndrome  
Roifman Syndrome  
Roifman-Chitayat Syndrome 
Rombo syndrome 
Sackey Sakati Aur Syndrome 
Schimke immuno-osseous dysplasia  
Sclerotylosis 
sebaceous gland neoplasm +   
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay  
skin benign neoplasm +   
skin cancer +   
Splenic Hypoplasia  
sweat gland neoplasm +   
T cell deficiency +   
T Cell Immunodeficiency Primary  
T-Cell OKT4 Deficiency  
T-Cell Receptor-Alpha/Beta Deficiency  
Thumb Agenesis, Short Stature, and Immunodeficiency 
Trichoepithelioma, Multiple Familial, 2  
Trichoepitheliomas, Multiple Desmoplastic 
Trichofolliculoma 
Tufted Angioma 
Tuftsin Deficiency 
WHIM syndrome  
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 

Synonyms
Primary IDs: MESH:C536855
Alternate IDs: OMIM:227850 ;   RDO:0002566

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