|
conventional dendritic cell
|
CL_0000990 |
|
|
dendritic cell
|
CL_0000451 |
|
|
Burkholderia mallei
|
NCBITaxon_13373 |
|
|
pseudomallei group
|
NCBITaxon_111527 |
|
|
agammaglobulinemia 5
|
DOID_0080588 |
[An agammaglobulinemia that has_material_basis_in heterozygous mutation in the LRRC8A gene on chromosome 9q34.] |
|
Klippel-Feil syndrome 1
|
DOID_0080589 |
[A Klippel-Feil syndrome that has_material_basis_in heterozygous mutation in the GDF6 gene on chromosome 8q22.] |
|
autosomal dominant Wolfram syndrome
|
DOID_0080584 |
[A Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has_material_basis_in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16.] |
|
Van Maldergem syndrome 1
|
DOID_0080585 |
[A Van Maldergem syndrome that has_material_basis_in homozygous mutation in the DCHS1 gene on chromosome 11p15.] |
|
Van Maldergem syndrome
|
DOID_0060238 |
[A syndrome characterized by facial abnormalities such as telecanthus, epicanthus, broad flattened nose, large inverted W-shaped mouth and malformed ears, malformed extremities such as camptodactyly, clinodactyly, interdigital webbing and joint hyperlaxity and mental retardation.] |
|
Van Maldergem syndrome 2
|
DOID_0080586 |
[A Van Malergem syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FAT4 gene on chromosome 4q28.] |
|
visceral muscle cell
|
CL_0008007 |
|
|
muscle cell
|
CL_0000187 |
|
|
congenital myasthenic syndrome 22
|
DOID_0080587 |
[A congenital myasthenic syndrome characterized by neonatal hypotonia, neonatal feeding problems, and nasal dysarthria and that has_material_basis_in homozygous or compound heterozygous mutation in the PREPL gene on chromosome 2p21.] |
|
Abnormality of the parathyroid physiology
|
HP_0011767 |
|
|
non-striated muscle cell
|
CL_0008000 |
|
|
microsporidiosis
|
DOID_4271 |
[An opportunistic mycosis that results_in systemic fungal infection in immunocompromised people, has_material_basis_in Microsporidia phylum members.] |
|
encephalitozoonosis
|
DOID_4270 |
[A microsporidiosis that is a zoonotic infectious disease results_in disseminated fungal infection in dogs, cats, hamsters, guinea pigs, rats, mice and humans, has_material_basis_in Encephalitozoon cuniculi, has_material_basis_in Encephalitozoon intestinalis or has_material_basis_in Encephalitozoon hellem.] |
|
obsolete bovine hemorrhagic syndrome
|
DOID_4273 |
[A viral infectious disease that results_in infection in cattle, has_material_basis_in Bovine viral diarrhea virus 2, which is transmitted_by ingestion of infected food, or transmitted_by nasal secretions. The infection has_symptom low grade fever, has_symptom bloody diarrhea, and has_symptom bleeding in the eyes.] |
|
obsolete Pestivirus infectious disease
|
DOID_4274 |
[A viral infectious disease that results_in infection in mammals, has_material_basis_in Pestivirus, which is transmitted_by contact with nasal secretions of an infected animal. The infection has_symptom diarrhea, has_symptom respiratory problems, and has_symptom bleeding disorder.] |
|
penis basal cell carcinoma
|
DOID_4277 |
[A basal cell carcinoma that is located_in the penis.] |