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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00649 | Ectodermal dysplasia, hair-nail type | Ectodermal dysplasia (ECTD), hair-nail type is a rare condition involving only tissues of ectodermal origin. Patients show complete alopecia and primitive nails. Autosomal recessive type has previously ... | Congenital malformation |
(ECTD4) KRT85 [HSA:3891] [KO:K07605] (ECTD7) KRT74 [HSA:121391] [KO:K07605] (ECTD9) HOXC13 [HSA:3229] [KO:K09298] (ECTD10A/10B) EDAR [HSA:10913] [KO:K05162] (ECTD13) KREMEN1 [HSA:83999] [KO:K23091] |
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| H00651 | Hypohidrotic ectodermal dysplasia | ... glands. HED is caused by defective epithelial-mesenchymal interaction that involves the Ectodysplasin/Edar/Edaradd signaling pathway. Congenital anhidrotic ectodermal dysplasia is a sex-linked disorder characterized ... | Congenital malformation |
(ECTD1) EDA [HSA:1896] [KO:K05480] (ECTD10A/10B) EDAR [HSA:10913] [KO:K05162] (ECTD11A/11B) EDARADD [HSA:128178] [KO:K23324] (ECTD12) KDF1 [HSA:126695] [KO:K23346] (ECTD15) CST6 [HSA:1474] [KO:K13902] |
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| H01863 |
Atopic myelitis Eosinophilic myelitis |
... in Japan. This disease has specific features of elevated serum IgE level, active reaction to mite or cedar pollen specific antigen and stepwise progression of mostly the sensory symptoms. Atopic myelitis ... | Immune system disease |
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