Name

HEMC Gene

hemangioma, capillary, hereditary

CMAL Gene

Capillary malformations, hereditary

SHFLD3 Gene

Split-hand/foot malformation with long bone deficiency 3

CCM2 Gene

cerebral cavernous malformation 2

This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]

SHFLD2 Gene

Split-hand/foot malformation with long deficiency 2

SHFL1 Gene

Split-hand/foot malformation with long bone deficiency 1

CCM2L Gene

cerebral cavernous malformation 2-like

Predicted to be involved in heart morphogenesis. Predicted to act upstream of or within several processes, including heart development; negative regulation of homotypic cell-cell adhesion; and positive regulation of fibroblast growth factor production. [provided by Alliance of Genome Resources, Mar 2025]

SHFM1P1 Gene

split hand/foot malformation (ectrodactyly) type 1 pseudogene 1

SHFM3 Gene

Split-hand/foot malformation 3

SHFM2 Gene

split hand/foot malformation (ectrodactyly) type 2

SHFM1 Gene

split hand/foot malformation (ectrodactyly) type 1

The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]

SHFM5 Gene

split hand/foot malformation (ectrodactyly) type 5

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