All terms in DOID

Label Id Description
spermatogenic failure 20 DOID_0070166 [A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP44 gene on chromosome 3q13.]
spermatogenic failure 21 DOID_0070163 [A male infertility due to acephalic spermatozoa that is characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22.]
spermatogenic failure 2 DOID_0070164 [A spermatogenic failure that is characterized by azoospermia or severe oligozoospermia that has_material_basis_in inversions on chromosome 1.]
hereditary sensory and autonomic neuropathy type 2 DOID_0070161 [A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood.]
hereditary sensory neuropathy DOID_0050548 [A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.]
hereditary sensory and autonomic neuropathy type 1 DOID_0070162 [A hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance.]
atypical hereditary sensory neuropathy DOID_0070160 [A hereditary sensory neuropathy characterized by late onset of sensory ataxia without ulcerating acropathy or autonomic abnormalities.]
Candida/Lodderomyces clade NCBITaxon_1535325
Debaryomycetaceae NCBITaxon_766764
spermatogenic failure 8 DOID_0070169 [A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33.]
spermatogenic failure 6 DOID_0070167 [A male infertility characterized by autosomal recessive inheritance of globozoospermia that has_material_basis_in mutation in the SPATA16 gene on chromosome 3q26.]
male infertility due to globozoospermia DOID_0112312 [A spermatogenic failure characterized by male infertility caused by the majority of spermatozoa having round heads and acrosome defects.]
spermatogenic failure 3 DOID_0070168 [A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21.]
spermatogenic failure 4 DOID_0070176 [A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive azoospermia caused by meiotic abnormalities that has_material_basis_in mutation in the SYCP3 gene on chromosome 12q23.]
spermatogenic failure 22 DOID_0070177 [A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13.]
spermatogenic failure 17 DOID_0070174 [A spermatogenic failure that is characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12.]
obsolete spermatogenic failure 9 DOID_0070175
spermatogenic failure 15 DOID_0070172 [A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia that has_material_basis_in mutation in the SYCE1 gene on chromosome 10q26.]
spermatogenic failure 7 DOID_0070173 [A spermatogenic failure that is characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13.]
spermatogenic failure 19 DOID_0070170 [A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25.]