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Human Disease and Mouse Model Detail
Human Disease Histiocytosis-Lymphadenopathy Plus Syndrome
OMIM ID: 602782
Human Phenotype Ontology associations
Synonyms Faisalabad Histiocytosis; H Syndrome; Histiocytosis and Lymphadenopathy with or without Cutaneous, Cardiac, and/or Endocrine Features, Joint Contractures, and/or Deafness; Histiocytosis with Joint Contractures and Sensorineural Deafness; HJCD; Hyperpigmentation, Cutaneous, with Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, and Hypogonadism with or without Hearing Loss; Pigmented Hypertrichosis with Insulin-Dependent Diabetes Mellitus; PHID; Rosai-Dorfman Disease, Familial; Sinus Histiocytosis and Massive Lymphadenopathy; SHML
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SLC29A3* Slc29a3   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory