Disease Browser
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Parent Node: Facies (D019066) | Parent Node: Fibrous Dysplasia of Bone (D005357) | Parent Node: Immunologic Deficiency Syndromes (D007153) | Parent Node: Neutropenia (D009503) | ..Starting node ..Lichtenstein syndrome (C535894)
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Sister Nodes: | ..3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA (OMIM:616271)
| ..ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES (OMIM:300835)
| ..Cyclic neutropenia (C536227)
| ..Febrile Neutropenia (D064147) 1
| ..Lazy Leukocyte Syndrome (C562721)
| ..Lichtenstein syndrome (C535894)
| ..Neutropenia, Lethal Congenital, with Eosinophilia (C564943)
| ..Neutropenia, Nonimmune Chronic Idiopathic, Adult (C564320)
| ..Neutropenia, severe chronic (C535815)
| ..NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE (OMIM:615285)
| ..NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE (OMIM:616022)
| ..NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE (OMIM:617014)
| ..Neutropenia, Severe Congenital, Autosomal Dominant 1 (C565969)
| ..Neutropenia, Severe Congenital, Autosomal Dominant 2 (C567748)
| ..Neutropenia, Severe Congenital, Autosomal Recessive 3 (C537592)
| ..Neutropenia, Severe Congenital, Autosomal Recessive 4 (C567260)
| ..Neutropenia, Severe Congenital, X-Linked (C564539)
| ..Onychotrichodysplasia and neutropenia (C537752)
| ..Poikiloderma with Neutropenia (C565820)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 7045 |
Name: | Lichtenstein syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D005357|MESH:D007153|MESH:D009503|MESH:D019066 |
TreeNumbers: | C05.116.099.708.375/C535894 |C15.378.553.546.184.564/C535894 |C20.673/C535894 |C23.550.291.812/C535894 |
Synonyms: | |
Slim Mappings: | Blood disease|Immune system disease|Musculoskeletal disease|Pathology (process) |
Reference: |
MedGen: C535894
MeSH: C535894
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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