MONDO_merge (183,974) Find_IDs Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
Label
Id
ACRDYS1 7044
ADOHR 7044
acrodysostosis 1 7044
infantile, type 1 polycystic kidney disease D017044
polycystic kidney and hepatic disease 1 (autosomal recessive) D017044
kidney, polycystic, autosomal recessive D017044
polycystic kidney, autosomal recessive D017044
polycystic kidney disease, infantile, type i D017044
infantile, type i polycystic kidney disease D017044
oculocutaneous albinism, minimal pigment type C537044
adult familial nephronophthisis-spastic quadriparesia syndrome 17044
albinism, minimal pigment type C537044
polycystic, autosomal recessive kidney D017044
minimal pigment type albinism C537044
minimal pigment type oculocutaneous albinism C537044