|
131
|
|
|
Hemoglobin subunit beta pseudogene 1 |
HBH1, HBHP, HBHps |
|
|
132
|
|
|
Hemoglobin subunit delta |
HBK |
|
|
133
|
|
|
Hemoglobin subunit epsilon 1 |
HBE |
|
|
134
|
|
|
Hemoglobin subunit gamma 1 |
HBG-T2, HBGA, HBGR, HSGGL1, PRO2979 |
|
|
135
|
|
|
Hemoglobin subunit gamma 2 |
HBG-T1, TNCY |
Anemia, Cyanosis, Hemoglobinopathy, Hemoglobinopathy toms river, Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome, Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome, Kidney failure, Methemoglobinemia, Prostatic neoplasms, Prostate cancer, Acute kidney insufficiency |
|
136
|
|
|
Hemoglobin subunit zeta |
HBAZ, HBZ-T1, HBZ1 |
|
|
137
|
|
|
Holocytochrome c synthase |
CCHL, LSDMCA1, MCOPS7, MLS |
Absence of septum pellucidum, Agenesis of corpus callosum, Ambiguous genitalia, Aphasia, Atrial septal defect, Cardiomyopathy, Cataract, Colpocephaly, Mandibular aplasia, Congenital anomaly of rectum, Congenital coloboma of iris, Congenital diaphragmatic hernia, Developmental delay, Disorder of eye, Dwarfism, Dysphasia, Epispadias, Glaucoma, Heart septal defects, Histiocytoid cardiomyopathy, Hydrocephalus, Hypertrophic cardiomyopathy, Hypertrophy of clitoris, Hypospadias, Imperforate anus, Male pseudohermaphroditism, Mental retardation, Microcephaly, Micrognathism, Microphthalmia with linear skin defects syndrome, Syndromic microphthalmia, Microphthalmos, Mitral valve prolapse, Overriding aorta, Ovotestis, Penis agenesis, Posterior embryotoxon, Respiratory failure, Retinal dysplasia, Retinal dystrophy, Retinitis pigmentosa, Sclerocornea, Specific learning disorder, Status epilepticus, Tricuspid valve insufficiency, Tricuspid valve prolapse, True hermaphroditism, Ventricular septal defect, VitritisView all (34 more) |
|
138
|
|
|
Host cell factor C1 |
CFF, HCF, HCF-1, HCF1, HFC1, MAHCX, MRX3, PPP1R89, VCAF, XLID3 |
Attention deficit hyperactivity disorder, Autism, Brachycephaly, Developmental delay, Dwarfism, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Liver neoplasms, Liver cancer, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Methylmalonic acidemia with homocystinuria, Microcephaly, Non-syndromic intellectual disability, x-linked, Obesity, Obsessive-compulsive disorder, Seizure, Syndactyly of the toesView all (5 more) |
|
139
|
|
|
HCK proto-oncogene, Src family tyrosine kinase |
AIPCV, JTK9, p59Hck, p61Hck |
|
|
140
|
|
|
Hematopoietic cell-specific Lyn substrate 1 |
CTTNL, HS1, lckBP1, p75 |
|
