Aliases: HE1, NP-C2, EDDM1.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Niemann-Pick Disease Type C |
untyped
Causative
|
mechanism: NPC1/NPC2-Mediated Cholesterol Egress Failure
|
| Tuberculosis |
untyped
Lysosomal cholesterol handling
|
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| Niemann-Pick disease, type C2 MONDO:0011873 | AR | Definitive 2022-04-05 |
Niemann-Pick Disease Type C
untyped
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.