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Disease association ontology term - MONDO:0015514 - hereditary endocrine growth disease

Term summary

ID
MONDO:0015514
Name
hereditary endocrine growth disease
Ontology or CV name
Disease association

Parents

Annotation

Disease association

MONDO:0009299 - 46 XX gonadal dysgenesis

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Genes:

MONDO:0012794 - ANE syndrome

References:

Genes:

MONDO:0008840 - ataxia telangiectasia

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Genes:

MONDO:0008980 - ataxia-hypogonadism-choroidal dystrophy syndrome

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Genes:

MONDO:0014455 - cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

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Genes:

MONDO:0009258 - classic galactosemia

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Genes:

MONDO:0013310 - congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency

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Genes:

MONDO:0032787 - holoprosencephaly 12 with or without pancreatic agenesis

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Genes:

MONDO:0026763 - holoprosencephaly 13, X-linked

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Genes:

MONDO:0030886 - holoprosencephaly 14

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Genes:

MONDO:0009514 - Laurence-Moon syndrome

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Genes:

MONDO:0010961 - obesity due to prohormone convertase I deficiency

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Genes:

MONDO:0030736 - ovarian dysgenesis 10

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Genes:

MONDO:0013689 - ovarian dysgenesis 3

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Genes:

MONDO:0054850 - ovarian dysgenesis 6

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Genes:

MONDO:0017312 - Perrault syndrome

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Genes:

MONDO:0013972 - Perrault syndrome 2

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Genes:

MONDO:0014126 - Perrault syndrome 4

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Genes:

MONDO:0976232 - Perrault syndrome 7

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MONDO:0014497 - polyendocrine-polyneuropathy syndrome

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MONDO:0014843 - premature ovarian failure 11

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MONDO:0054862 - premature ovarian failure 15

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Genes:

MONDO:0030870 - premature ovarian failure 17

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Genes:

MONDO:0958035 - premature ovarian failure 23

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Genes:

MONDO:0010350 - premature ovarian failure 2A

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Genes:

MONDO:0014321 - premature ovarian failure 8

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