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#620711 - LEUKOENCEPHALOPATHY, PORPHYRIA-RELATED; LENCEP
Gene summaries Genetic tests Medical literature
#620705 - SPERMATOGENIC FAILURE 89; SPGF89
#620704 - ENCEPHALOPATHY, PORPHYRIA-RELATED; ENCEP
#620680 - LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 5; CGL5
#620646 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 59; COXPD59
*620590 - RADICAL S-ADENOSYL METHIONINE DOMAIN-CONTAINING PROTEIN 1; RSAD1
Cytogenetic locations: 611466
#620534 - NEUTROPENIA, SEVERE CONGENITAL, 10, AUTOSOMAL RECESSIVE; SCN10
Cytogenetic locations: ######
#620483 - VARIEGATE PORPHYRIA, CHILDHOOD-ONSET; VPCO
Cytogenetic locations: #H.##
*620476 - MRT4 HOMOLOG, RIBOSOME MATURATION FACTOR; MRTO4
Cytogenetic locations: ########"#H#
#620455 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND SPEECH DELAY, WITH OR WITHOUT SEIZURES; NEDHSS
#620417 - SPASTIC PARAPLEGIA 90B, AUTOSOMAL RECESSIVE; SPG90B
Cytogenetic locations: BCL2-like
#620416 - SPASTIC PARAPLEGIA 90A, AUTOSOMAL DOMINANT; SPG90A
*620391 - POLY(ADP-RIBOSE) POLYMERASE FAMILY, MEMBER 16; PARP16
#620372 - HYPERSULFATURIA; HYSULF
Cytogenetic locations: @#{###
#620364 - COMBINED LOW LDL AND FIBRINOGEN; CLDLFIB
#620359 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 7; MC5DN7
Cytogenetic locations: #Z####
#620358 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4A; MC5DN4A
Cytogenetic locations: between
*620329 - SOLUTE CARRIER FAMILY 44, MEMBER 5; SLC44A5
Cytogenetic locations: ########u###
*620328 - SOLUTE CARRIER FAMILY 44, MEMBER 3; SLC44A3
Cytogenetic locations: ##########K#
#620323 - SPASTIC PARAPLEGIA 70, AUTOSOMAL RECESSIVE; SPG70
Cytogenetic locations: 606634
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