Disease association ontology term - MONDO:0031199 - inherited interstitial lung disease
Term summary
ID
MONDO:0031199
Name
inherited interstitial lung disease
Ontology or CV name
Disease association
Definition
An instance of interstitial lung disease that is caused by an inherited modification of the individual's genome.
Parents
is_a
hereditary disease
is_a
interstitial lung disease
Annotation
Disease association
MONDO:0010926
-
familial hypocalciuric hypercalcemia 3
References:
PB_REF:0000006
Genes:
aps2 (SPBC685.04c)
MONDO:0011871
-
Niemann-Pick disease type B
References:
PB_REF:0000006
Genes:
SPBC713.07c
MONDO:0957261
-
pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7
References:
PB_REF:0000006
Genes:
naf1 (SPBC30D10.15)
MONDO:0957263
-
pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8
References:
PB_REF:0000006
Genes:
pot1 (SPAC26H5.06)
MONDO:0957294
-
pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9
References:
PB_REF:0000006
Genes:
nop10 (SPAP27G11.13c)
MONDO:0013878
-
pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1
References:
PB_REF:0000006
Genes:
trt1 (SPBC29A3.14c)
MONDO:0013879
-
pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2
References:
PB_REF:0000006
Genes:
ter1 (SPNCRNA.214)
MONDO:0014612
-
pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4
References:
PB_REF:0000006
Genes:
tri1 (SPBC29A10.09c)
MONDO:0030690
-
pulmonary fibrosis and/or bone marrow failure, telomere-related, 6
References:
PB_REF:0000006
Genes:
ssb1 (SPBC660.13c)
MONDO:0100215
-
Rajab interstitial lung disease with brain calcifications 1
References:
PB_REF:0000006
Genes:
frs1 (SPAC23A1.12c)
MONDO:0100220
-
Rajab interstitial lung disease with brain calcifications 2
References:
PB_REF:0000006
Genes:
frs2 (SPAC3G9.06)
