| Name |
|---|
CILD4 GeneCiliary dyskinesia, primary, 4 |
PSC GeneCholangitis, primary sclerosing |
PIFO Geneprimary cilia formation Enables cytoskeletal protein binding activity and enzyme binding activity. Involved in positive regulation of kinase activity. Predicted to be located in ciliary basal body and trans-Golgi network. [provided by Alliance of Genome Resources, Mar 2025] |
IPOX GeneIntestinal pseudoobstruction, neuronal, primary idiopathic |
PPH2 Geneprimary pulmonary hypertension 2 |
PLSA1 GenePrimary lateral sclerosis, adult, 1 |
MYD88 Genemyeloid differentiation primary response 88 This gene encodes a cytosolic adapter protein that plays a central role in the innate and adaptive immune response. This protein functions as an essential signal transducer in the interleukin-1 and Toll-like receptor signaling pathways. These pathways regulate that activation of numerous proinflammatory genes. The encoded protein consists of an N-terminal death domain and a C-terminal Toll-interleukin1 receptor domain. Patients with defects in this gene have an increased susceptibility to pyogenic bacterial infections. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010] |
PRD Geneprimary retinal dysplasia |
GLC3B Geneglaucoma 3, primary infantile, B |
GLC3C Geneglaucoma 3, primary congenital, C |
HDLCQ14 GeneHypoalphalipoproteinemia, primary |
LOC102724175 Genemembrane primary amine oxidase-like |
CILD8 GeneCiliary dyskinesia, primary, 8 |
PBC3 GeneBiliary cirrhosis, primary, 3 |
PBC2 GeneBiliary cirrhosis, primary, 2 |
PBC5 GeneBiliary cirrhosis, primary, 5 |
PBC4 GeneBiliary cirrhosis, primary, 4 |
DPCD Genedeleted in primary ciliary dyskinesia homolog (mouse) This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia. [provided by RefSeq, Jul 2016] |
SSD GeneSpeech-sound disorder |
OHDS GeneOrthostatic hypotensive disorder of Streeten |
MAFD9 GeneMajor affective disorder-9, susceptibility to |
MAFD8 GeneMajor affective disorder-8, susceptibility to |
MAFD5 GeneMajor affective disorder 5 |
MAFD1 Genemajor affective disorder 1 |
MAFD3 GeneMajor affective disorder 3, early onset |
MDD2 GeneMajor depressive disorder 2 |
MDD1 GeneMajor depressive disorder |
MAFD2 Genemajor affective disorder 2 |
MAFD4 GeneMajor affective disorder 4 |
MAFD6 GeneMajor affective disorder 6 |
ADHD2 GeneAttention deficit-hyperactivity disorder, susceptibility to, 2 |
HDL3 GeneHuntington-like neurodegenerative disorder 2 |
PAND1 GenePanic disorder 1 |
PAND2 Genepanic disorder 2 |
PAND3 Genepanic disorder 3 |
BDET GeneBleeding disorder, east Texas type |
ADHD4 GeneAttention deficit-hyperactivity disorder, susceptibility to, 4 |
ADHD5 GeneAttention deficit-hyperactivity disorder, susceptibility to, 5 |
ADHD6 GeneAttention deficit-hyperactivity disorder, susceptibility to, 6 |
ADHD1 GeneAttention deficit-hyperactivity disorder, susceptibility to, 1 |
ADHD3 GeneAttention deficit-hyperactivity disorder, susceptibility to, 2 |
SCZD8 Geneschizophrenia disorder 8 |
SCZD7 Geneschizophrenia disorder 7 |
SCZD6 Geneschizophrenia disorder 6 |
SCZD1 Geneschizophrenia disorder 1 |
SCZD3 Geneschizophrenia disorder 3 |
SCZD10 Geneschizophrenia disorder 10 (periodic catatonia) |
NDNC9 GeneNail disorder, nonsyndromic congenital, 9 |
CLA3 Genecerebellar ataxia 3 (cerebellar parenchyma disorder 1) |
SCZD2 Geneschizophrenia disorder 2 |
PDR Genepigment disorder, reticulate |