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atypical hereditary sensory neuropathy
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DOID_0070160 |
[A hereditary sensory neuropathy characterized by late onset of sensory ataxia without ulcerating acropathy or autonomic abnormalities.] |
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Candida/Lodderomyces clade
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NCBITaxon_1535325 |
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Debaryomycetaceae
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NCBITaxon_766764 |
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spermatogenic failure 8
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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.] |
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susceptibility to coronary heart disease 2
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MIM_608316 |
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spermatogenic failure 6
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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.] |
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male infertility due to globozoospermia
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DOID_0112312 |
[A spermatogenic failure characterized by male infertility caused by the majority of spermatozoa having round heads and acrosome defects.] |
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susceptibility to coronary heart disease 4
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MIM_608318 |
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spermatogenic failure 3
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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.] |
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spermatogenic failure 4
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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.] |
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spermatogenic failure 22
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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.] |
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spermatogenic failure 17
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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.] |
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obsolete spermatogenic failure 9
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DOID_0070175 |
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spermatogenic failure 15
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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.] |
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spermatogenic failure 7
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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.] |
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spermatogenic failure 19
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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.] |
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spermatogenic failure 12
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DOID_0070171 |
[A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26.] |
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spermatogenic failure 10
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DOID_0070178 |
[A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13.] |
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spermatogenic failure 14
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DOID_0070179 |
[A spermatogenic failure that is characterized by male infertility due to azoospermia with sperm maturation arrest in the spermatid stage that has_material_basis_in mutation in the ZMYND15 gene on chromosome 17p13.] |
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animal food product
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FOODON_00004242 |
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