Name

CILD4 Gene

Ciliary dyskinesia, primary, 4

PSC Gene

Cholangitis, primary sclerosing

PIFO Gene

primary 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 Gene

Intestinal pseudoobstruction, neuronal, primary idiopathic

PPH2 Gene

primary pulmonary hypertension 2

PLSA1 Gene

Primary lateral sclerosis, adult, 1

MYD88 Gene

myeloid 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 Gene

primary retinal dysplasia

GLC3B Gene

glaucoma 3, primary infantile, B

GLC3C Gene

glaucoma 3, primary congenital, C

HDLCQ14 Gene

Hypoalphalipoproteinemia, primary

LOC102724175 Gene

membrane primary amine oxidase-like

CILD8 Gene

Ciliary dyskinesia, primary, 8

PBC3 Gene

Biliary cirrhosis, primary, 3

PBC2 Gene

Biliary cirrhosis, primary, 2

PBC5 Gene

Biliary cirrhosis, primary, 5

PBC4 Gene

Biliary cirrhosis, primary, 4

DPCD Gene

deleted 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 Gene

Speech-sound disorder

OHDS Gene

Orthostatic hypotensive disorder of Streeten

MAFD9 Gene

Major affective disorder-9, susceptibility to

MAFD8 Gene

Major affective disorder-8, susceptibility to

MAFD5 Gene

Major affective disorder 5

MAFD1 Gene

major affective disorder 1

MAFD3 Gene

Major affective disorder 3, early onset

MDD2 Gene

Major depressive disorder 2

MDD1 Gene

Major depressive disorder

MAFD2 Gene

major affective disorder 2

MAFD4 Gene

Major affective disorder 4

MAFD6 Gene

Major affective disorder 6

ADHD2 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

HDL3 Gene

Huntington-like neurodegenerative disorder 2

PAND1 Gene

Panic disorder 1

PAND2 Gene

panic disorder 2

PAND3 Gene

panic disorder 3

BDET Gene

Bleeding disorder, east Texas type

ADHD4 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 4

ADHD5 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 5

ADHD6 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 6

ADHD1 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 1

ADHD3 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

SCZD8 Gene

schizophrenia disorder 8

SCZD7 Gene

schizophrenia disorder 7

SCZD6 Gene

schizophrenia disorder 6

SCZD1 Gene

schizophrenia disorder 1

SCZD3 Gene

schizophrenia disorder 3

SCZD10 Gene

schizophrenia disorder 10 (periodic catatonia)

NDNC9 Gene

Nail disorder, nonsyndromic congenital, 9

CLA3 Gene

cerebellar ataxia 3 (cerebellar parenchyma disorder 1)

SCZD2 Gene

schizophrenia disorder 2

PDR Gene

pigment disorder, reticulate